Jaw osteosarcoma and pregnancy: a rare coexistence

Osteosarcoma of the jaw represents less than 1% of all head and neck malignancies. This malignancy in pregnant women occurs in one per 1000 deliveries. We report a case of a 29-year-old woman, in the 33rd week of gestation, who presented with an expansive tumor destroying the maxillary alveolar bone, histologically composed of pleomorphic, round, spindle, or epithelioid cells and osteoid/chondroid matrix. Upon final diagnosis of osteosarcoma, the lesion was excised. To the best of our knowledge, only 10 cases of jaw osteosarcoma in pregnant women have been reported to date in the English language literature. The use of ancillary examinations, malignancy diagnosis, and cancer treatment can be challenging during pregnancy. Knowledge about jaw osteosarcoma in pregnancy can increase healthcare providers' awareness, avoid delays and misdiagnosis and potentially improve maternal and neonatal outcomes.

Preeclampsia as an inaugural manifestation of primary hyperparathyroidism: A case report / Pré-eclâmpsia como manifestação inaugural de hiperparatiroidismo primário: Um caso clínico

Abstract Primary hyperparathyroidism is an endocrine disorder characterized by hypercalcemia and elevated or inappropriately normal levels of parathyroid hormone. The diagnosis is based on a biochemical evaluation, and a neck ultrasound is the first choice during pregnancy to access the parathyroid glands. Manifestations during pregnancy are rare and can be present with life-threatening complications, so the diagnosis is challenging. The conservative treatment is limited, and there is not enough data about its safety and efficacy during pregnancy. Surgery is the only curative treatment, and a parathyroidectomy performed during the second or third trimesters is considered safe. Recently, some authors suggested an association between primary hyperparathyroidism and preeclampsia. We describe a case of preeclampsia with severe features at 27 weeks of gestational age. The severity of the preeclampsiamotivated an early termination of the pregnancy by cesarean section. During the postpartum period, the patient presented life-threatening complications, such as severe hypercalcemia and acute pancreatitis. An ultrasound exam found two parathyroid nodules, suggestive of parathyroid adenomas. The patient recovered after the pharmacological correction of the calcemia levels.

Resumo O hiperparatiroidismo primário é umdistúrbio endócrino caraterizado pela elevação do cálcio sérico associada a níveis de paratormona elevados ou inapropriadamente normais. O diagnóstico é baseado em análises bioquímicas, e, na gravidez, o exame de imagem de primeira linha é a ecografia cervical. É uma doença rara na gravidez, e pode se apresentar com complicações ameaçadoras de vida, pelo que o seu diagnóstico é desafiante. O tratamento médico disponível é limitado, havendo poucos dados relativos à sua eficácia e segurança na gravidez. A cirurgia é o único tratamento curativo, e pode ser realizada no segundo ou terceiro trimestres. Tem sido descrita uma relação entre hiperparatiroidismo primário e pré-eclâmpsia. Apresenta-se um caso de uma grávida de 27 semanas com pré-eclâmpsia com critérios de gravidade, o que obrigou ao término da gravidez por cesariana. Verificou-se agravamento clínico no período pós-parto, com aparecimento de complicações graves, tais como hipercalcemia grave e pancreatite aguda. Ecograficamente, constataram-se duas massas paratiróideias sugestivas de adenomas da paratiroide. A doente recebeu tratamento médico, e teve melhora apenas após a correção dos níveis de cálcio sérico.

Miocardiopatia não compactada em gestante com linfoma não Hodgkin. Relato de caso / Non-compaction cardiomyopathy in pregnant women with non-Hodgkin lymphoma: a case report

A miocardiopatia não compactada é uma doença congênita rara, que pode ocorrer isoladamente ou associada a outros defeitos, por falha no processo de compactação das fibras miocárdicas, resultando na persistência de trabeculações e recessos profundos. A associação entre a miocardiopatia não compactada e gestação é incomum na literatura, assim como a relação com macroglobulinemia de Waldenstrom, um tipo de linfoma não Hodgkin. Descrevemos aqui a rara associação destas três patologias. Trata-se de paciente do sexo feminino, sem antecedentes hematológicos, neoplasias ou cardiopatias, que procurou o serviço com queixa de astenia progressiva, dores no corpo, perda ponderal importante e anemia. Na investigação diagnóstica, a imunoeletroforese de proteína constatou pico monoclonal em IgM Kappa, com inventário medular por imunofenotipagem e biópsia de medula óssea com Kappa+, CD19+, CD20+, CD38 e CD79b, confirmando diagnóstico de neoplasia de linfócitos B maduros. Na terapêutica, optou-se pelo esquema de primeira linha com dexametasona, rituximabe e ciclofosfamida (DRC) − este último considerado agente alquilante cardiotóxico. Em triagem pré-quimioterápica, o eletrocardiograma mostrou alteração da repolarização ventricular anterosseptal. O ecocardiograma transtorácico evidenciou trabeculações excessivas no ápice do ventrículo esquerdo, sugerindo não compactação do miocárdio. A ressonância magnética confirmou o diagnóstico. Foi iniciada terapia com metoprolol e ácido acetilsalisílico. Todavia, após o último ciclo de terapia quimioterápica, paciente descobriu gravidez (G1P1A0). O período gestacional e o puerpério evoluíram sem manifestações clínicas de insuficiência cardíaca, em classe funcional I (New York Heart Association), mesmo com redução da fração de ejeção do ventrículo esquerdo ao ecocardiograma transtorácico. (AU)

Non-compaction cardiomyopathy is a rare congenital disease that can occur in isolation or associated with other defects, due to failure in compaction of myocardial fiber, resulting in persistence of myocardial trabeculations and deep recesses. The association between non-compaction cardiomyopathy and gestation, as well as the relationship with Waldenstrom's macrobulinemia, a type of Non-Hodgkin's Lymphoma (NHL), are not common in the literature. This study describes the rare association of these three pathologies. This is the case of a female patient with no history of hematological, neoplastic, or heart diseases, who sought the service with complaints of progressive weakness, body aches, important weight loss, and anemia. During the diagnostic investigation, protein immunoelectrophoresis showed a monoclonal peak in IgM Kappa monoclonal gammopathy, with a medullary inventory by immunophenotyping and bone marrow biopsy with Kappa+, CD19+, CD20+, CD38 and CD79b, confirming the diagnosis of mature B-cell lymphocyte neoplasm. The first line therapy chosen was dexamethasone, rituximab, and cyclophosphamide (CKD), with the latter being considered a cardiotoxic alkylating agent. At pre-chemotherapy screening, the electrocardiogram showed an alteration of the anteroseptal ventricular repolarization. Transthoracic echocardiography (ETT) showed excessive trabeculations at the apex of the left ventricle (LV), suggesting no compaction of the myocardium. The magnetic resonance imaging confirmed the diagnosis.Therapy with metoprolol and acetylsalicylic acid was started. However, after the last cycle of chemotherapy, the patient found she was pregnant (G1P1A0). The gestational and puerperium period progressed with no clinical manifestations of heart failure, in functional class I (New York Heart Association), albeit the reduction of the ejection fraction of the left ventricular shown in the transthoracic echocardiography. (AU)

Luteoma del embarazo. Reporte de caso / Luteoma of pregnancy. A case report

Luteoma of pregnancy is an infrequent non-neoplastic pathology of the ovary. It is usually an incidental finding during the evaluation of a pregnant patient in the third trimester or during a cesarean section. Occasionally, it may raise suspicion of cancer, resulting in unnecessary surgical resection of the ovary. We present the case of a 34-year-old woman who was in her third pregnancy and during the cesarean section, a 9 cm tumor of the right ovary was incidentally found and resected. The histological study was compatible with luteoma of pregnancy.

El luteoma del embarazo es una patología no neoplásica del ovario, de incidencia poco frecuente. Suele presentarse como hallazgo incidental durante la evaluación de una paciente embarazada en el tercer trimestre o en el momento del acto quirúrgico de una cesárea. En ocasiones, puede llevar a sospechar una neoplasia maligna, derivando así en una resección quirúrgica innecesaria del ovario. Presentamos el caso de una mujer de 34 años que cursaba su tercera gestación y a quien, durante la cesárea, se le halló una tumoración ovárica derecha de 9 cm de diámetro que fue resecada. El estudio histológico fue compatible con luteoma del embarazo.

Coloretal cancer in pregnant women / Cancro colorectal na mulher grávida

Abstract Background Colorectal cancer in pregnancy is a rare pathology with limited high-grade evidence available for guidance. The diagnosis of CRC in pregnant women is usually delayed, and once diagnosis is made, challenges exist as treatment options may be limited. Objective The study aims to highlight the importance of early investigation of symptomatic patients during pregnancy, as well as to update treatment and prognosis in CRC. Methods A literature search in PubMed database, including articles from 2006 to 2016 and cross-research articles with the initial research. Results Pregnancy can limit and contraindicate the utilization of standard diagnostic and therapeutic tools, which in particular can hamper the liberal use of colonoscopy and CT. Physical evaluation and abdominal US are first recommended; besides, MRI or CT may be used, only in indicated cases. Surgery is the main stay of treatment but radiotherapy and chemotherapy have significant role in posterior management of tumour. Conclusions Many studies are needed in order to achieve development in CRC pathogenesis during pregnancy as well as in treatment outcomes. The potential curative treatment of the disease should be the main aim of treatment when considering CRC in pregnancy. However, it is crucial to adapt the treatment to each patient, taking into account conscious decision on pregnancy further management.

Resumo Introdução O cancro colorretal na gravidez é uma patologia rara, com limitada evidência científica para orientação terapêutica. O diagnóstico de cancro coloretal em mulheres grávidas é tardio e, quando o diagnóstico é feito, as opções de tratamento podem ser limitadas. Objetivo O objetivo deste estudo é ressalvar a importância da investigação precoce de pacientes sintomáticas durante a gravidez, assim como avaliar os atuais métodos de tratamento e prognóstico no CCR. Métodos A pesquisa bibliográfica foi realizada na base de dados PubMed, incluindo artigos a partir de 2006 até 2016, assim como artigos de pesquisa cruzada com os artigos iniciais. Resultados A gravidez pode limitar e contra-indicar a utilização de ferramentas de diagnóstico e terapêuticas convencionais, assim como dificultar o uso indiscriminado de colonoscopia e tomografia computadorizada. A avaliação física e a ecografia abdominal são a primeira linha para diagnóstico. No entanto, em casos selecionados, a ressonância magnética ou a tomografia computadorizada também podem ser usadas. A cirurgia é o gold-standard mas a radioterapia e a quimioterapia assumem um papel cada vez mais relevante no tratamento multidisciplinar destes tumores. Discussão Como os sintomas abdominais são comuns na gravidez e cancro coloretal pode simulá-los, o diagnóstico diferencial entre estas duas patologias é crucial, já que intervenções precoces podem ser curativas. Após diagnóstico, o seguimento das grávidas deve ser individualizado, dependendo de vários fatores. Porém, já que atualmente o tratamento do cancro é possível na gravidez, a probabilidade de sobrevivência da paciente não deve ser diminuída devido ao diagnóstico tardio. Conclusões Mais estudos são necessários para saber mais acerca da patogénese do cancro coloretal na gravidez, assim como os resultados após tratamento. O potencial objetivo é o tratamento oncológico do cancro coloretal. No entanto, é crucial adaptar o tratamento a cada paciente, tendo em conta a sua decisão consciente acerca da continuação da gravidez.

Tumor del estroma gastrointestinal en mujer gestante joven / Gastrointestinal stromal tumor in young pregnant woman: case report

Paciente mujer de 28 años de edad, con gestación de 14 semanas, natural y procedente de Ilo, Moquegua. Acudió con tiempo de enfermedad de 4 días con hematemesis, melenas, epigastralgia y síncope. Antecedente de resección colónica por peritonitis debido a un traumatismo hace 20 años; cuadro de hemorragia digestiva alta hace 3 años; abuelos paternos fallecidos de cáncer gástrico; gastritis crónica diagnosticada desde los 19 años de edad. Dentro de los estudios laboratoriales hemoglobina de 9,2. En el estudio de endoscopia digestiva alta se evidencia ausencia de hemorragia digestiva alta activa, una gran tumoración en cuerpo proximal hacia curvatura mayor y pared posterior, de aproximadamente 8 cm de diámetro, de aspecto lobulado, con la mayor parte de la superficie mucosa indemne, áreas de ulceración de 2 a 3 mm cubiertas de fibrina (de las cuales se toma biopsias), de consistencia dura, signo de la carpa (positivo) y signo del cojín (negativo). No se pudo realizar estudios de imagen como resonancia magnética o tomografía debido a la gestación. En la ecografía abdominal completa sólo se reportó esteatosis hepática de I grado. Los resultados de biopsia endoscópica indicaron proliferación celular de características epitelioides con atipia. Se realizó inmunohistoquímica indicando CD 117 (positivo), CD 34 (negativo), Ki 67 (positivo 1%). El diagnóstico final fue un tumor del estroma gastrointestinal de tipo epitelioide con tasa mitótica menor de 1%. Finalmente se realizó resección quirúrgica del tumor, en la que además se encontró 3 implantes de hasta 1 cm de diámetro en peritoneo que cubrían la superficie pancreática. Presentamos el caso por ser esta una inusual presentación de este tipo de tumor

Female patient, 28 years old, with a gestation of 14 weeks, natural and from Ilo-Moquegua. Came with a time of disease 4 days with hematemesis, melena, epigastric pain and syncope. Background of colonic resection for peritonitis due to trauma 20 years ago; upper gastrointestinal bleeding three years ago; paternal grandparents died of gastric cancer; chronic gastritis diagnosed from 19 year old. In laboratory studies hemoglobin of 9.2. In the upper gastrointestinal endoscopy was found absence of active upper gastrointestinal bleeding, a large tumor in proximal body toward greater curvature and posterior wall, 8 cm in diameter approximately, lobed appearance, with most of the mucosal surface unscathed is evidence, areas of ulceration of 2-3 mm covered with fibrin (biopsies taken), hard consistency, tent sign (positive) and cushionsign (negative). Imaging studies such as MRI or CT were not possible due to the pregnancy. In the complete abdominal ultrasound only grade I hepatic steatosis was reported. The results of endoscopic biopsy showed cell proliferation ofepithelioid characteristics with atypia. Immunohistochemistry was performed indicating CD117 (positive), CD 34 (negative), Ki 67 (positive 1%). The final diagnosis was a gastrointestinal stromal tumor epithelioid type with mitotic rate lower of 1%. Finally, surgical resection of the tumor was performed in which addition of 3 implants was found up to 1 cm in diameter in pancreatic peritoneum covering surface. We present the case as this is an unusual presentation of this tumor

Carcinoma renal cromófobo: uma causa rara de hipertensão na gravidez / Chromophobe renal cell carcinoma: a rare cause of hypertension in pregnancy

O carcinoma de células renais, em particular o tipo cromófobo, é uma patologia rara na idade fértil, o que explica a pouca informação disponível na literatura. Os autores apresentam o caso de uma mulher de 37 anos, multípara, com hipertensão arterial de novo, de difícil controle e hematúria às 10 semanas de gravidez, tendo o estudo etiológico do quadro hipertensivo demostrado a existência de um tumor renal. Às 17 semanas de gravidez, a doente foi submetida à nefrectomia esquerda, tendo a cirurgia decorrido sem intercorrências. A histologia demostrou tratar-se de um carcinoma do subtipo cromófobo. O restante da gravidez decorreu sem complicações, com perfil tensional controlado, com um parto vaginal de termo com um recém-nascido saudável.

Renal cell carcinoma, particularly the chromophobe type, is a rare pathology in childbearing age, and consequently, in literature, few cases during pregnancy have been reported. The authors present the case of a 37-year-old, multiparous woman, with de novo high blood pressure of difficult control, and hematuria at 10-week gestation. The etiological study of the hypertensive disorder has demonstrated the existence of a renal tumor. The patient underwent left radical nephrectomy at 17-week gestation. Histology was compatible with chromophobe subtype renal cell carcinoma. The remaining pregnancy period progressed with no complications, with controlled tension profile, and resulted in spontaneous vaginal delivery of a healthy infant at term.

Feocromocitoma e gravidez: Relato de caso e revisão atualizada / Pheochromocytoma and pregnancy: A case report and review

Resumo O feocromocitoma é um tumor da adrenal produtor de catecolaminas, sendo causa rara de hipertensão arterial na gravidez. Sua prevalência em hipertensos é de 0,2%, e em 0,002% das gestações. Acompanhamos gestante hipertensa de 24 anos, branca, tercigesta, admitida na 33ª semana com emergência hipertensiva, indicada cesárea devido a sofrimento fetal, evoluindo com edema agudo de pulmão no pós-parto imediato. Submetida à videolaparoscopia após 13 dias por dor abdominal aguda, sem achado significativo. No pós-operatório, devido à hipertensão arterial grave e refratária, suspeitou-se de feocromocitoma, confirmado por exames bioquímicos e de imagem. Realizada adrenelectomia unilateral com cura da hipertensão. A anatomia patológica e a imunohistoquímica confirmaram o diagnóstico. Concluímos que casos atípicos de hipertensão na gravidez devem ser precocemente investigados e diferenciados da pré-eclâmpsia. Apesar da baixa prevalência, o feocromocitoma na gravidez aumenta consideravelmente a morbimortalidade materno-fetal e o seu reconhecimento e tratamento precoces mudam drasticamente o seu desfecho.

Abstract Pheochromocytoma is a catecholamine-producing adrenal tumor, being a rare cause of hypertension in pregnancy. It's prevalence in hypertensive patients is 0.2%, and 0.002% of pregnancies. We follow hypertensive pregnant 24 year old on her third pregnancy, admitted to 33 weeks with hypertensive emergency cesarean section indicated by fetal distress evolving with acute pulmonary edema in the post-partum period. Indicated laparoscopy after 13 days for acute abdominal pain, with no significant finding. In the postoperative, due a severe and resistant hypertension, suspected of pheochromocytoma and confirmed by biochemical tests and imaging. Performed unilateral adrenelectomia with cure of hypertension. The pathology and immunohistochemistry confirmed the diagnosis. We conclude that atypical cases of hypertension in pregnancy should be investigated early and differentiated pre-eclampsia. Despite the low prevalence, pheochromocytoma in pregnancy increases fetal maternal morbidity and mortality and the early recognition and treatment drastically change their outcome.

Cardiac myxoma in pregnancy: a comprehensive review / Mixoma cardíaco na gravidez: revisão abrangente

AbstractObjective:Cardiac myxoma in pregnancy is rare and the clinical characteristics of this entity have been insufficiently elucidated. This article aims to describe the treatment options and the risk factors responsible for the maternal and feto-neonatal prognoses.Methods:A comprehensive search of the literature of cardiac myxoma in pregnancy was conducted and 44 articles with 51 patients were included in the present review.Results:Transthoracic echocardiography was the most common diagnostic tool for the diagnosis of cardiac myxoma during pregnancy. Cardiac myxoma resection was performed in 95.9% (47/49); while no surgical resection was performed in 4.1% (2/49) patients (P=0.000). More patients had an isolated cardiac myxoma resection in comparison to those with a concurrent or staged additional cardiac operation [87.2% (41/47) vs. 12.8% (6/47), P=0.000]. A voluntary termination of the pregnancy was done in 7 (13.7%) cases. In the remaining 31 (60.8%) pregnant patients, cesarean section was the most common delivery mode representing 61.3% and vaginal delivery was more common accounting for 19.4%. Cardiac surgery was performed in the first, second and third trimester in 5 (13.9%), 14 (38.9%) and 17 (47.2%) patients, respectively. No patients died. In the delivery group, 20 (76.9%) neonates were event-free survivals, 4 (15.4%) were complicated and 2 (7.7%) died. Neonatal prognoses did not differ between the delivery modes, treatment options, timing of cardiac surgery and sequence of cardiac myxoma resection in relation to delivery.Conclusion:The diagnosis of cardiac myxoma in pregnancy is important. Surgical treatment of cardiac myxoma in the pregnant patients has brought about favorable maternal and feto-neonatal outcomes in the delivery group, which might be attributable to the shorter operation duration and non-emergency nature of the surgical intervention. Proper timing of cardiac surgery and improved cardiopulmonary bypass conditions may result in even better maternal and feto-neonatal survivals.

ResumoObjetivo:Mixoma cardíaco durante a gravidez é raro e as características clínicas dessa entidade não foram suficientemente esclarecidas. Este artigo tem como objetivo descrever as opções de tratamento e os fatores de risco responsáveis pelo prognóstico materno e fetal-neonatal.Métodos:Foi realizada uma pesquisa abrangente na literatura sobre mixoma cardíaco durante a gravidez e 44 artigos com 51 pacientes foram incluídos na presente revisão.Resultados:Ecocardiografia transtorácica foi a ferramenta de diagnóstico mais comum para o diagnóstico de mixoma cardíaco durante a gravidez. Ressecção do mixoma cardíaco foi realizada em 95,9% (47/49); enquanto não foi realizada ressecção cirúrgica em 4,1% (2/49) dos pacientes (P=0,000). Mais pacientes tiveram ressecção isolada do mixoma cardíaco em comparação com aqueles com operação cardíaca concomitante ou adicional [87,2% (41/47) vs. 12,8% (6/47), P=0,000]. A interrupção voluntária da gravidez foi feita em 7 (13,7%) casos. Nas restantes 31 (60,8%) pacientes grávidas, a cesariana foi o modo de parto mais comum, representando 61,3% e parto vaginal contabilizou 19,4%. A cirurgia cardíaca foi realizada no primeiro, segundo e terceiro trimestre em 5 (13,9%), 14 (38,9%) e 17 (47,2%) pacientes, respectivamente. Nenhuma paciente morreu. No grupo de parto, 20 (76,9%) recém-nascidos sobreviveram livres de eventos, 4 (15,4%) tiveram complicações e 2 (7,7%) morreram. Os prognósticos neonatais não diferiram entre os modos de parto, opções de tratamento, tempo de cirurgia cardíaca e sequência de ressecção mixoma cardíaco em relação ao parto.Conclusão:O diagnóstico de mixoma cardíaco durante a gravidez é importante. Tratamento cirúrgico de mixoma cardíaco em pacientes grávidas trouxe resultados favoráveis para as mães e os neonatos no grupo de parto, o que pode ser atribuído à duração mais curta da operação e à natureza não emergencial da intervenção cirúrgica. O momento adequado da cirurgia cardíaca e melhoria das condições de circulação extracorpórea podem resultar em sobrevivência materna e do feto-neonato ainda melhor.

The Korean guideline for cervical cancer screening / 부인종양

The incidence rate of cervical cancer in Korea is still higher than in other developed countries, notwithstanding the national mass-screening program. Furthermore, a new method has been introduced in cervical cancer screening. Therefore, the committee for cervical cancer screening in Korea updated the recommendation statement established in 2002. The new version of the guideline was developed by the committee using evidence-based methods. The committee reviewed the evidence for the benefits and harms of the Papanicolaou test, liquid-based cytology, and human papillomavirus (HPV) testing, and reached conclusions after deliberation. The committee recommends screening for cervical cancer with cytology (Papanicolaou test or liquid-based cytology) every three years in women older than 20 years of age (recommendation A). The cervical cytology combined with HPV test is optionally recommended after taking into consideration individual risk or preference (recommendation C). The current evidence for primary HPV screening is insufficient to assess the benefits and harms of cervical cancer screening (recommendation I). Cervical cancer screening can be terminated at the age of 74 years if more than three consecutive negative cytology reports have been confirmed within 10 years (recommendation D).

Embarazo adolescente no diagnosticado: análisis de un evento centinela / Inadvertent adolescent pregnancy: a sentinel analysis

Un evento centinela es un suceso inesperado que implica la muerte, o una lesión física o psicológica grave. En este caso, el evento fue el embarazo adolescente no diagnosticado antes de la indicación de tratamientos o métodos de diagnóstico potencialmente dañinos. El equipo tratante realizó un análisis de causa-raíz en el que se identificaron las siguientes causas: a) sesgo pediátrico: no pensar en el comportamiento sexual adolescente, cuestionarios incompletos, insuficiente formación en entrevistas con adolescentes, b) factores sociales: cuestiones legales, recomendaciones ambiguas con respecto a la sexualidad, c) factores hospitalarios: ausencia de guías clínicas en el tema, d) factores del paciente: historia oculta de abuso sexual, barreras culturales, falta de confianza. Antes de realizar procedimientos potencialmente teratogénicos en pacientes adolescentes, se debería efectuar una prueba diagnóstica de embarazo, con independencia de los resultados negativos de pruebas de embarazo de ciclos menstruales previos

A sentinel event is an unexpected occurrence involving death or serious physical or psychological injury, or the risk thereof.The sentinel event identified was undiagnosed adolescent pregnancy before the indication of potentially harmful treatments or diagnostic methods. The team performed a root -cause analysis where the following causes were identified: a) Paediatrician bias: not thinking about adolescent sexual behaviour, incomplete questionnaires, insufficient training in adolescent interviews. b) Social factors: legal issues, ambiguous contraceptive recommendations. c) Hospital factors: lack of guidelines for counselling adolescents. d) Host risk factors: cultural barriers, lack of confidence. Regardless of any previous negative pregnancy test results, any time that a new potentially harmful procedure is indicated in a fertile female patient, a test of pregnancy diagnosed might be performed.

Diagnóstico de câncer de mama na gestação: há dificuldades adicionais / Diagnosis of breast cancer in pregnancy: are there additional difficulties

O câncer de mama gestacional (CMG) é caracterizado como todo câncer de mama diagnosticado durante a gravidez ou até um ano após o parto. Na gravidez, as alterações fisiológicas da mama prejudicam a interpretação da mamografia nos casos em que é solicitada, já que não faz parte do rastreamento no pré-natal. Além disso, a pouca prática do autoexame das mamas dificulta o diagnóstico. Este trabalho foi desenvolvido por meio de uma revisão de literatura com uso de 18 artigos nacionais e 8 internacionais disponíveis em bancos de dados virtuais, tais como: Bibliomed, BVS, Scielo, Bireme, Lilacs, Guideline. Conforme a literatura, as variáveis acima citadas são limitadoras da detecção precoce do CMG. Destaca-se a importância de se mostrar que há associação de fatores que impedem a descoberta precoce da doença, tornando o estadiamento tardio e comprometendo a sobrevida das mulheres. Sendo o câncer de mama um problema de saúde pública, faz-se necessária uma abordagem especial da gestante para que haja a detecção dessa doença em seu início

The gestational breast cancer (CMG) is characterized as all breast cancer diagnosed during pregnancy or within one year after delivery. During pregnancy, physiological changes affect the interpretation of breast mammography where it is required, since it is not part of the prenatal screening. In addition the low frequency practice of self-examination of breast makes diagnosis difficult. This work was developed through a literature review by using 18 national articles and 8 international ones, all available in virtual databases such as Bibliomed, Scielo, Bireme, Lilacs, Guideline. Acording to literature, these variables are limiting the early detection of CMG. We emphasize the importance of showing that there is an association of factors that impede the early detection of disease, making the later stage, and compromising the survival of women. As breast cancer is a public health problem, a special approach to the pregnant woman is required so that there can be an early detection of the disease

large unilocular mucinous cystadenoma in third trimester of pregnancy

Ovarian malignancy is the second most common gynaecological malignancy diagnosed during pregnancy. A grand multipara, aged 30 years presented with gestational amenorrhea with abdominal discomfort and breathlessness for last 15 days. Sonographic examination demonstrated a huge, unilocular ovarian cyst and an alive fetus of about 30 weeks gestation. Intraoperative findings were huge left ovarian cyst [42x40x20 cm] with straw coloured mucinous fluid. Left salpingo-oophorectomy was performed followed by peritoneal washings and omental biopsy. Histopathology revealed mucinous cystadenomas with inflammatory changes in omentum and no malignant cells in peritoneal washings. She delivered vaginally a female baby of 3.5 kg at 38 weeks with good Apgar score

Cáncer de colon metastásico diagnosticado durante el tercer trimestre de la gestación / Metastatic colon cancer diagnosed at 31 weeks of gestation

El cáncer de colon durante la gestación es una patología poco frecuente, con una incidencia entre el 0,07 y el 0,1 por ciento. El diagnóstico precoz es complejo y el pronóstico suele ser malo por tratarse con frecuencia de procesos en estado avanzado. Presentamos el caso de una paciente de 38 años, diagnosticada de ade-nocarcinoma de colon transverso metastásico en la semana 31 de gestación. Realizamos una revisión en relación al diagnóstico y manejo de esta patología.

Colonic cancer during pregnancy is a rare event, whit incidence between 0.07 and 0.1 percent. Early diagnosis is difficult and prognosis is severe as it generally made at an advanced stage. We report a case of metastasic adenocarcinoma of the transverse colon in a 38-year-old pregnant patient diagnosed at 31 weeks of gestation. The problem of diagnosis as well as management of this pathology is discussed.

Manejo del cáncer de recto durante el embarazo / Treatment of rectal cancer associated with pregnancy

El cáncer de recto tiene baja incidencia en la mujer embarazada, su diagnóstico durante el embarazo suele ser tardío, pues sus síntomas son similares a los propios de la gestación. El diagnóstico tardío le confiere un peor pronóstico, aunque el embarazo en si mismo no afecta la evolución natural de la enfermedad. El pronóstico perinatal no se ve afectado por la neoplasia misma, incluso en casos con metástasis múltiples, sino por el tratamiento indicado. El manejo dependerá fundamentalmente del estadío de la neoplasia y de la edad gestacional. Se revisa la literatura médica acerca del cáncer rectal asociado con el embarazo y se plantea un protocolo de manejo.

Rectal cancer has low incidence in the pregnant women. Its diagnosis during pregnancy is usually delayed, since cancer symptoms are quite similar to normal symptoms of gestation. Delayed diagnosis confers worse prognosis, although pregnancy itself does not affect natural evolution of the disease. The perinatal outcome is not affected by the neoplasia, even in cases with multiple metastases, but may be affected by the treatment. The treatment of rectal cancer will depend of the stage of the neoplasia and gestational age. We review published data regarding rectal cancer associated with pregnancy and propose a management protocol.

Abordaje diagnóstico-terapéutico del cáncer de mama asociado con embarazo: actualización 2010 / Diagnostic-therapeutic approach to breast cancer associated with pregnancy: update 2010

Definido como la presencia de cáncer de la glándula mamaria durante el periodo de gestación y hasta un año después de la resolución del embarazo, el cáncer de mama asociado con el embarazo representa dilemas, controversias y contradicciones éticas en su abordaje diagnósticoterapéutico; son temas de controversia el pronóstico, el método diagnóstico y la interrupción del embarazo. El objetivo de esta comunicación es mostrar las recomendaciones en el diagnóstico-tratamiento en estas pacientes, con base en evidencia, y discutir temas controvertidos como el papel del mapeo linfático, estudios preterapéuticos y momentos ideales del tratamiento. Aunque poco frecuente, se considera que su prevalencia se incrementará lentamente, no solo porque la neoplasia en sí misma tiene una frecuencia cada día mayor sino porque en las sociedades occidentales las mujeres se embarazan por primera vez a edades mayores, cuando el cáncer mamario es más frecuente. Al igual que en la población general, el cáncer de mama es la neoplasia más frecuente en mujeres embarazadas y cuando se diagnostica surgen interrogantes que en ocasiones no tienen respuesta basada en evidencia científica; en numerosas ocasiones, las decisiones terapéuticas se toman con base en el conocimiento obtenido en el tratamiento del cáncer mamario en la mujer no embarazada. Aplicar rutinariamente la nueva tecnología diagnóstico-terapéutica teniendo la seguridad de no afectar al binomio madre-hijo es una decisión difícil de tomar. El principal objetivo del tratamiento de una mujer embarazada con cáncer de mama es obtener el estándar del resultado oncológico y preservar la integridad del producto.

Breast cancer associated with pregnancy (defined as the presence of breast cancer during gestation extending until a year after the resolution of the pregnancy) represents controversial ethical dilemmas and contradictions in its diagnostic and therapeutic approach. Diagnostic methods and the role of pregnancy interruption are controversial subjects for prognosis. Our objective was to discuss the recommendations for diagnosis and treatment for these patients using evidence-based medicine and to discuss controversial subjects such as the role of lymphatic mapping, pre-therapeutic studies and appropriate treatment schedule. Fortunately, the prevalence of breast cancer during pregnancy is low. It is generally considered, however, that this prevalence will slowly increase because of two factors: 1) breast cancer is showing an increasing prevalence and 2) in Western societies the age when a woman becomes pregnant for the first time has increased, which is also associated with the age when breast cancer frequency rises. As in the general population, breast cancer is the most frequent neoplasm in pregnant women. When diagnostic questions arise that sometimes do not have an answer based on scientific evidence, therapeutic decisions are often made based on knowledge acquired in breast cancer treatment of nonpregnant women. To routinely apply new diagnostic/therapeutic technologies with the safety of protecting the pregnancy is a difficult decision to make. In the end, the main objective of treatment of a pregnant woman with breast cancer is to maintain the standard of the desired oncological results while preserving the integrity of the fetus.

Presentation of retinoblastoma in pregnancy.

A 22-year-old female in her third trimester of pregnancy was referred to our department for sudden loss of vision with a painful blind eye. It was diagnosed as retinoblastoma clinically and radiologically. Histopathology and immunohistochemistry confirmed the diagnosis. This case is one of its kind because retinoblastoma occurring during pregnancy had not been reported in literature so far.

Prognosis for patients diagnosed with pregnancy-associated breast cancer: a paired case-control study / Prognóstico para pacientes grávidas portadoras de câncer de mama: estudo caso-controle pareado

CONTEXT AND OBJECTIVE: Previous studies have suggested that the occurrence of pregnancy concomitantly with a diagnosis of breast cancer may affect the evolution of the neoplasia. The present study aimed to compare pregnancy-associated breast cancer (PABC) patients with non-pregnant cancer patients (controls) in relation to the time taken to diagnose the disease, tumor characteristics and mortality. DESIGN AND SETTING: A retrospective, paired case-control study was conducted at the Hospital da Santa Casa de Misericórdia and Centro de Quimioterapia Antiblástica e Imunoterapia in Belo Horizonte, Brazil. METHODS: The study involved 87 PABC and 252 control patients. The influence of covariables (interval between first symptoms and diagnosis, tumor histology, size of primary tumor, distant metastasis, grade of malignancy, hormone receptor status and axillary lymph node involvement) and the pregnancy variable on overall survival was investigated using univariate and multivariate analyses. RESULTS: The median overall survival for PABC patients of 30.1 months (95 percent confidence interval, CI: 19.4-40.9 months) was significantly different (P = 0.005) from that of the control group (53.1 months; 95 percent CI: 35.1-71.0 months). The cumulative overall survivals after five and ten years were, respectively, 29.7 and 19.2 percent for PABC patients, and 47.3 and 34.8 percent for control patients (P = 0.005). Tumor size, grade of malignancy, distant metastasis and pregnancy were independent factors that significantly modified disease prognosis. CONCLUSIONS: Pregnancy was an independent prognostic factor. The overall survival of PABC patients was shorter than that of non-pregnant patients.

CONTEXTO E OBJETIVO: Estudos prévios sugerem que a ocorrência de gravidez simultaneamente com o diagnóstico de câncer de mama pode afetar a evolução da neoplasia. O presente estudo objetivou comparar pacientes com câncer de mama associado à gravidez (PABC) e pacientes com câncer não grávidas (controles) com relação ao tempo decorrido até o diagnóstico de câncer, características tumorais e mortalidade. TIPO DE ESTUDO E LOCAL: Estudo retrospectivo, tipo caso-controle pareado, foi conduzido no Hospital da Santa Casa de Misericórdia e Centro de Quimioterapia Antiblástica e Imunoterapia em Belo Horizonte, Brasil. MÉTODOS: O estudo envolveu 87 pacientes PABC e 252 controles. A influência das covariáveis (intervalo entre os primeiros sintomas e diagnóstico, histologia do tumor, tamanho do tumor primário, metástase a distância, grau de malignidade, dosagem de receptor hormonal e acometimento dos linfonodos axilares) e da variável gravidez sobre a sobrevida global foram avaliados através de análises univariada e multivariada. RESULTADOS: A mediana da sobrevida global para as pacientes PABC de 30,1 meses (intervalo de confiança, IC 95 por cento: 19,4-40,9 meses) foi significativamente (P = 0,005) diferente daquela dos controles (53,1 meses; IC 95 por cento: 35,1-71,0 meses). A sobrevida global acumulada após 5 e 10 anos foi 29,7 e 19,2 por cento no grupo PABC e 47,3 e 34,8 por cento nos controles. Tamanho do tumor, grau de malignidade, metástase a distância e gravidez foram fatores independentes e significativamente condicionantes do prognóstico da doença. CONCLUSÕES: A gravidez foi um fator independente para o prognóstico da doença. A sobrevida global das pacientes PABC foi mais curta do que aquela dos controles.

[Immature t eratoma of the ovary and pregnancy]

Composing of less than 1%of all ovarian cancers, immature teratoma is a malignancy that mainly affects the young. Immature teratoma of the ovary together with pregnancy is rare. To nor knowledge, this association was reported only in twelve cases. We Report two cases of immature teratoma of the ovary diagnosed during pregnancy and their respective issue. Observation 1st case. A 28 years old woman gravida 1 with an immature teratoma of the ovary discovered during delivery by caesarean section. The treatment was conservative including salpingo-oophorectomy, omentectomy. aortic lymph node dissection and appendectomy. This patient had a second pregnancy with a good outcome. She delivered by cacsarean section in order to perform radical treatment: hysterectomy and oophorectomy of the remaining ovary. 2nd case. A 22 years old woman gravida I with adnexal mass diagnosed during an ultrasonography exam at 15 weeks gestation. A conservative treatment was indicated, including salpingo oophorectomy, omentectomy, aortic lymph node dissection, appendectomy and biopsy of the resnaining ovary. The patient bad a normal vaginal delivery. Immature teratoma is graded from 1 to 3. The management of this association is discussed, but it takes in consideration the surgical staging, the grade and the secretion of alpha FP. Conservative treatment without associating chemotherapy can be tempted in tumours with a stade Al and a low grade

Prevalencia de displasia cervical en embarazadas en el Hospital Universitario de Monterrey: Nuevo León, México / Prevalence of cervical dysplasia in pregnant women at the Hospital Universitario de Monterrey

Objetivo. Determinar la prevalencia de displasia cervical en mujeres embarazadas. Método. Estudio observacional, longitudinal, prospectivo, en el cual se analizaron los resultados de 250 pacientes embarazadas que acudieron a control prenatal en el Hospital Universitario Dr. José Eleuterio González, Monterrey, Nuevo León, México, en el período enero 2007 a julio de 2008. Resultados. Se analizaron 36 citologías anormales (14,4 por ciento), las cuales reportaron ASCUS 3,2 por ciento (n=8), LIEBG 8 por ciento (n=20), LIEAG 2,4 por ciento (n=6) y CaCu 0,8 por ciento (n=2). La prevalencia de displasia cervical confirmada por biopsia fue 5,6 por ciento (n=14). Conclusiones. Se recomienda realizar la citología cervical a toda paciente embarazada, para la detección y tratamiento oportuno de las displasias cervicales.

Objective. To evaluate the prevalence of cervical dysplasia among pregnant women. Method. We conducted an observational, longitudinal, prospective study, that analyzed the results of 250 cervical smears of preg-nant patients that attended the Obstetrics consult of the University Hospital in Monterrey, Mexico, between January 2007 and July 2008. Results: 36 abnormal smears were analyzed (14.4 percent). Showing ASCUS in 3.2 percent (n=8), LSIL in 8 percent (n=20), HSIL in 2.4 percent (n=6) and AIS in 0.8 percent (n=2). The prevalence of cervical dys-plasia confirmed by biopsy was 5.6 percent (n=14). Conclusions: We recommend performing cervical smears to all pregnant women for detection and appropriate treatment of cervical dysplasia.