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1.
Journal of Peking University(Health Sciences) ; (6): 370-374, 2023.
Article in Chinese | WPRIM | ID: wpr-986864

ABSTRACT

Independent primary uterine and cervical adenocarcinoma are rare and difficult to identify their origins, which makes treatment decision difficult. A 46-year-old female with endometrioid carcinoma and adenocarcinoma, human papilloma virus (HPV)-associated of the uterine cervix was reported. The patient presented with increased menstrual flow, contact bleeding and watery leucorrhea for more than one year, and the imaging findings showed abnormal uterine morphology, irregular margins, and multiple abnormal signals in uterine cavity and myometrium, which suggested multiple leiomyomas of the uterus. The signal intensity in the right muscle layer was markedly enhanced, suggesting a smooth muscle tumor of uncertain malignant potential. A large number of cystic hypointensity was seen in the cervix, and multiple cysts were considered. The initial preoperative diagnosis was multiple leiomyoma of the uterus, and a hysterectomy operation was planned. During the operation, the uterus was sent for frozen sections. There was a mass in the endometrium of the fundus, with a soft grayish-red cut surface and a clear border with the myometrium, and there was a grayish-white nodule in the cervix with a hard grayish-white cut surface. The two masses were well demarcated from each other, and the distance between them was 30 mm. The result of the frozen sections indicated the malignant tumor of the endometrium, and the extended hysterectomy+pelvic lymphadenectomy+partial resection of the greater omentum was performed. After the operation, the paraffin sections were sent to the Department of Pathology of the Peking University Third Hospital for histochemistry, POLE gene sequencing and HPV RNAscope tests, and the final diagnosis was a synchronous endometrioid carcinoma (POLE-mutant according to the WHO classification) and an adenocarcinoma, HPV-associated of the uterine cervix. Now the patient had been treated with 2 cycles of chemotherapy and her condition was fine. Through the analysis of the histological, immunohistochemical and molecular detection results of this case, the importance of applying HPV RNAscope and TCGA molecular typing in the diagnosis of cervical adenocarcinomas and endometrial carcinomas was emphasized. At the same time, gynecologists should not blindly rely on intraoperative frozen sections, and should pay attention to preoperative pathological examination, and make appropriate operation methods according to the results in order to prevent passivity in the surgery.


Subject(s)
Humans , Female , Middle Aged , Carcinoma, Endometrioid/pathology , Uterine Cervical Neoplasms/pathology , Papillomaviridae , Papillomavirus Infections/pathology , Uterus/pathology , Adenocarcinoma/diagnosis
2.
Indian J Cancer ; 2022 Sep; 59(3): 337-344
Article | IMSEAR | ID: sea-221698

ABSTRACT

Background: Cancer of unknown primary (CUP) origin is cancer in which malignant cancer cells are in the body but the site of cancer where it began is unknown. Detailed incidence and time trends of these cancers, specific to various regions in India is needed. This paper aims to summarize and report the incidence of other and unknown (O&U) cancers across India in 27 population-based cancer registries (PBCRs) and to study the trends among these cancers using joinpoint regression analysis. Methods: Data on the incidence of CUP were obtained from the published reports on 27 PBCRs of the National Cancer Registry Programme (NCRP) of the Indian Council of Medical Research (ICMR). A joinpoint regression model was used to analyze the long-term trends of incidence related to CUP based on published data from PBCRs between 1986 and 2014. Annual Percent Change (APC) in incidence rate was estimated for various registries. Results: The northeast region had the highest age-adjusted rate (AAR) for both men (1.76–29.7) and women (1.99–14.68). Age-specific rate (ASR) for both men (39.8–855.7) and women (48.2–470.4) was highest in the northeast region. There is an increase in the incidence rate for all six major registries over the past decade with an exception of women in the Delhi Cancer Registry. There is a decline in incidence rate by 0.14 during 1990–2012 in the female population of the Delhi registry. Conclusion: The increasing incidence trends of CUP is a matter of concern for the healthcare professionals and researchers. There is a need for research and advanced and improved diagnostic tools for the improvement of the status of O&U cancers.

3.
Int. arch. otorhinolaryngol. (Impr.) ; 26(1): 125-131, Jan.-Mar. 2022. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1364917

ABSTRACT

Abstract Introduction All patients with a new head and neck squamous cell carcinoma (HNSCC) undergo diagnostic panendoscopy as part of the screening for synchronous second primary tumors. It includes a pharyngolaryngoscopy (PLS), a tracheobronchoscopy and esophagoscopy, and a stomatoscopy. Rigid techniques are risky, with long learning curves. Objective We propose a precise description of the panendoscopy protocol. We include an optimization of the PLS technique that completes the flexible esophagoscopy when rigid esophagoscopy isn't performed. Methods The present retrospective observational study includes 122 consecutive patients with a new primary HNSCC who underwent traditional panendoscopy and the new PLS technique between January 2014 and December 2016. A two-step procedure using a Macintosh laryngoscope and a 30° telescope first exposes panoramically the larynx, the upper trachea, and the oropharynx; then, in a second step, the hypopharynx is exposed down to the upper esophageal sphincter. Broncho-esophagoscopy is performed with a rigid and flexible scope. Results In total, 6 (5%) patients presented synchronous tumors (3 in the esophagus, 2 in the oral cavity, and 1 in the larynx 1). Rigid endoscopy was complicated by 2 (1,6%) dental lesions, and had to be completed with a flexible scope in 38 (33%) cases for exposition reasons. The two-step PLS offered a wide-angle view of the larynx, upper trachea, and oroand hypopharynx down to the sphincter of the upper esophagus. The procedure was easy, reliable, safe, repeatable, and effectively completed the flexible endoscopies. Conclusion Rigid esophagoscopy remains a difficult procedure. Two-step PLS combined with flexible broncho-esophagoscopy offers good optical control.

4.
Autops. Case Rep ; 12: e2021389, 2022. graf
Article in English | LILACS-Express | LILACS | ID: biblio-1383894

ABSTRACT

ABSTRACT Nasopharyngeal carcinoma (NPC) is a malignant tumor rarely found in the head and neck, representing about 1% of all malignancies. The main treatment for NPC is radiation therapy, which is often given in combination with chemotherapy. However, such treatment may lead to long‐term complications, including second primary tumors (SPTs) and osteoradionecrosis (ORN). Both complications have similar radiological characteristics, which can lead to erroneous diagnoses. This paper describes a case of a second primary tumor in a patient after 20 years of radiotherapy in the area where a previous extraction was performed, mimicking an osteoradionecrosis process.

5.
Coluna/Columna ; 20(1): 64-67, Jan.-Mar. 2021. tab, graf
Article in English | LILACS | ID: biblio-1154015

ABSTRACT

ABSTRACT Objective: The goal of the study was to report the prevalence of spinal metastasis with unknown primary tumor, clinical features, treatment results and patient survival. Methods: A retrospective evaluation of 103 patients with spinal metastasis and epidural compression, who underwent surgical treatment between March 2009 and August 2015. The prevalence of metastatic spinal tumor with unknown primary tumor was evaluated, as well clinical features, survival and treatment results. Results: Of 103 patients with spinal metastasis and epidural compression, seven patients (6.8%) with unknown primary tumor site were identified; five (71.4%) male and two (28.6%) female, with ages ranging from 37 to 67 years (50.7 years). The metastasis was located in the thoracic spine in six of the patients (85.7%) and in the cervical spine in one (14.3%). The mean survival time was 44.8 days. Conclusion: Spinal metastasis with unknown primary tumor was found in 6.8% of patients. The prognosis and outcomes were poor, and patients had poor survival rates. Level of evidence III; Experimental study.


RESUMO Objetivo: O objetivo deste estudo foi relatar a prevalência de metástases vertebrais em tumores primários desconhecidos, suas características clínicas, resultados do tratamento e sobrevida dos pacientes. Métodos: Avaliação retrospectiva de 103 pacientes com metástase da coluna vertebral e compressão epidural, submetidos a tratamento cirúrgico entre março de 2009 e agosto de 2015. Avaliou-se a prevalência de tumores metastáticos vertebrais com tumor primário desconhecido, assim como as características clínicas, a sobrevida e os resultados do tratamento. Resultados: Dos 103 pacientes com metástase vertebral e compressão epidural, foram identificados sete pacientes (6,8%) com tumor primário de origem desconhecida; cinco pacientes (71,4%) eram do sexo masculino e dois pacientes (28,6%) do sexo feminino, com idades variando de 37 a 67 anos (50,7 anos). A localização da metástase vertebral era na coluna torácica em seis pacientes (85,7%) e na coluna cervical em um paciente (14,3%). A média de sobrevida dos pacientes foi de 44,8 dias. Conclusões: As metástases vertebrais com tumor primário de origem desconhecida foram observadas em 6,8% dos pacientes. O prognóstico e os resultados foram ruins, e os pacientes tiveram sobrevida bastante baixa. Nível de evidencia III; Estudo Comparativo Retrospectivo.


RESUMEN Objetivo: El objetivo de este estudio fue relatar la prevalencia de metástasis vertebrales en tumores primarios desconocidos, sus características clínicas, resultados del tratamiento y sobrevida de los pacientes. Métodos: Evaluación retrospectiva de 103 pacientes con metástasis de la columna vertebral y compresión epidural, sometidos a tratamiento quirúrgico entre marzo de 2009 y agosto de 2015. Se evaluó la prevalencia de tumores metastásicos con tumor primario desconocido, así como las características clínicas, la sobrevida y los resultados del tratamiento. Resultados: De los 103 pacientes con metástasis vertebral y compresión epidural, fueron identificados siete pacientes (6,8%) con tumor primario de origen desconocido; cinco pacientes (71,4 %%) eran del sexo masculino y dos (28,6%) del sexo femenino, con edades variando de 37 a 67 años (50,7 años). La localización de la metástasis vertebral era en la columna torácica en seis pacientes (85,7%) y en la columna cervical en un paciente (14,3%). El promedio de sobrevida de los pacientes fue de 44,8 días. Conclusiones: Las metástasis vertebrales con tumor primario de origen desconocido fueron observadas en 6,8% de los pacientes. El pronóstico y los resultados fueron malos y los pacientes tuvieron sobrevida bastante baja. Nivel de evidencia III; Estudio Comparativo Retrospectivo.


Subject(s)
Humans , Spine , Neoplasms, Unknown Primary , Neoplasm Metastasis
6.
Article | IMSEAR | ID: sea-213118

ABSTRACT

Second or multiple primary malignancies is very rare and the number of patients diagnosed with multiple primary cancers has recently been increasing due to the improved diagnostic techniques. Herein we report a very rare case of synchronous double primary cancer of the stomach and thyroid gland for the 39 years old lady who presented with a short period of abdominal pain were diagnosed to have an invasive adenocarcinoma with signet ring differentiation of the stomach by gastroscopy and biopsy. Computed tomography and positron emission tomography scan showed high fludeoxyglucose uptake of the thyroid gland were biopsied to confirm the malignancy. underwent initially for radical distal gastrectomy followed by adjuvant chemotherapy and interval total thyroidectomy. Although Synchronous tumors are defined as ≥2 primary tumors occurring within 6 months of diagnosis of the first primary tumor, our case was discovered concomitantly at the first presentation of the patient. The prognosis of patients with multiple primary cancers can be determined independently by the stage of each cancer.

7.
Rev. colomb. gastroenterol ; 34(4): 416-420, oct.-dic. 2019. graf
Article in Spanish | LILACS | ID: biblio-1092970

ABSTRACT

Resumen Una de las características inusuales del melanoma cutáneo es la capacidad de metastatizar en el intestino delgado. A menudo se diagnostica durante la autopsia, en la cual se ha encontrado depósitos metastásicos en el 50%-60% de los casos, pero menos del 2% al 4% de los pacientes con diagnóstico de melanoma tiene metástasis gastrointestinal (GI) durante el curso de la enfermedad y entre el 4%-9% de casos de melanoma GI tiene un primario desconocido. La rápida identificación y resección del melanoma en el tracto digestivo podría mejorar la tasa de supervivencia en aquellos pacientes en los que se presentan complicaciones, como obstrucción intestinal. Se presenta un caso clínico de melanoma gastrointestinal de origen primario desconocido. El porcentaje de este tipo de casos es poco frecuente. La paciente presentó cuadro clínico de náuseas, hiporexia, epigastralgia, fatiga, parestesias en región dorsal derecha y disminución de 9 kilogramos en 3 semanas. Le realizaron tomografía computarizada (TAC) de abdomen contrastado, que reportó 3 lesiones en hígado de predominio isodenso en el parénquima, con algunas áreas de menor densidad al interior, localizadas en los segmentos 2, 5, 7 y 8 del hígado al que se le realizó la biopsia. Se llevó a cabo endoscopia de vías digestivas altas con biopsia de 2 lesiones hiperpigmentadas en la segunda porción de duodeno. El examen histopatológico de las biopsias evidenció melanoma maligno. Se excluyeron todas las localizaciones típicas de melanoma primario durante el procedimiento diagnóstico.


Abstract One of the unusual characteristics of cutaneous melanoma is its ability to metastasize in the small intestine. It is often diagnosed during autopsies of cutaneous melanoma patients. Metastatic deposits have been found in 50% to 60% of these autopsies, but less than 2% to 4% of patients diagnosed with melanoma have gastrointestinal metastasis during the course of the disease. Between 4% and 9% of gastrointestinal melanoma cases have unknown primary tumors. Rapid identification and resection of melanoma in the digestive tract could improve the patient survival rate and prevent complications such as intestinal obstructions from occurring. We present a rare clinical case of gastrointestinal melanoma of unknown primary origin. The patient had a clinical picture of nausea, hyporexia, epigastralgia, fatigue, paresthesias in the right dorsal region and had lost nine kilograms in three weeks. An abdominal CT scan showed three predominantly isodense liver lesions in the parenchyma, with some areas of lower density located in segments 2,5,7 and 8 of the liver. These were biopsied. Upper digestive tract endoscopy took biopsy samples of two hyperpigmented lesions in the second portion of the duodenum. Histopathological examination showed malignant melanoma. All typical locations of primary melanoma were excluded during the diagnostic procedure.


Subject(s)
Humans , Female , Middle Aged , Neoplasms, Unknown Primary , Gastrointestinal Tract , Melanoma , Neoplasm Metastasis
8.
ACM arq. catarin. med ; 48(2): 122-127, abr.-jun. 2019.
Article in Portuguese | LILACS-Express | LILACS | ID: biblio-1023474

ABSTRACT

O sarcoma de células claras (SCC) é um tumor maligno descrito em 1965. Essa neoplasia representa menos de 1% dos sarcomas, sendo que esses já representam 1% dos cânceres. O SCC geralmente acomete adultos jovens e apresenta-se como uma massa profunda, localizada em extremidades, próxima a tendões e aponeuroses. O prognóstico é geralmente reservado, com sobrevida em 5 anos de 47%. Nesse artigo é relatado o caso de uma paciente de 38 anos com uma neoplasia metastática sem sítio primário conhecido, que se apresentou inicialmente como uma tumoração em região inguinal. A microscopia da lesão revelou neoplasia composta por células epitelioides de grande porte, citoplasma eosinófilo, comumente contendo pigmento, e núcleo pleomórfico. A imuno-histoquímica (IHQ) foi negativa para pancitoqueratina e desmina e positiva para melanossoma, melan-A, vimentina, S-100 e positiva em 40% das células para Ki-67. O tratamento paliativo foi realizado com quimioterapia e radioterapia. A paciente evoluiu à óbito seis meses após o diagnóstico. O SCC é uma neoplasia maligna rara de difícil diagnóstico diferencial. O exame histológico e mesmo a IHQ podem não conseguir diferenciá-lo do melanoma metastático. A pesquisa da translocação t(12;22)(q13;q13) pode ajudar a diferenciá-los, porém não é feita rotineiramente. Assim, o diagnóstico foi firmado pelas características clínicas, em correlação com a patologia. Devido a sua raridade não há um tratamento clínico bem estabelecido. Considerando que a terapia para o melanoma metastático está em evolução e é cada vez mais efetiva, é importante que o diagnóstico diferencial preciso com o SCC seja feito.


Clear cell sarcoma (CCS) is a malignant tumor described in 1965. This neoplasm accounts for less than 1% of sarcomas, which already account for 1% of cancers. CCS usually affects young adults and presents as a deep mass, located at extremities, near tendons and aponeuroses. The prognosis is generally limited, with a 5-year survival of 47%. In this article, it is reported a case of a 38-year-old patient with metastatic neoplasia of unknown primary site, which initially presented as an inguinal tumor. Microscopy revealed neoplasia composed of large epithelioid cells, eosinophilic cytoplasm, commonly containing pigment, and pleomorphic nucleus. Immunohistochemistry (IHC) was negative for pan-cytokeratin and desmin and positive for melanosome, melan-A, vimentin, S-100 and positive in 40% of cells for Ki-67. Palliative treatment was performed with chemotherapy and radiotherapy. The patient died six months after the diagnosis. CCS is a rare malignant neoplasm of difficult differential diagnosis. Histological examination and even IHC may not be able to differentiate it from metastatic melanoma. The translocation t (12; 22) (q13; q13) may help to differentiate them but it is not routinely researched for. Therefore, the diagnosis was established by correlation of clinical and pathological characteristics. Due to its rarity, there is no well-established clinical treatment. Considering that therapy for metastatic melanoma is evolving and is increasingly effective, it is important that a precise differential diagnosis with SCC is done.

9.
West Indian med. j ; 68(1): 64-67, 2019. tab, graf
Article in English | LILACS | ID: biblio-1341833

ABSTRACT

ABSTRACT A patient had both ovaries affected by clearly demarcated colliding tumour masses of different gross appearance, histological features and immunohistochemical profiles, corresponding to bilateral collision papillary serous high-grade adenocarcinoma and fibrothecoma. Despite the applied chemotherapy, it led to a lethal outcome for the patient nearly a year after the surgery. Bilateral ovarian tumours raise the question of whether they are primary tumours or metastases. Simultaneous bilateral occurrence of surface epithelial tumours with other types of ovarian tumours is rare. Therefore, it poses a great challenge in proper differential diagnostics.


RESUMEN Una paciente tenía ambos ovarios afectados por masas tumorales en colisión, claramente demarcadas. Las mismas mostraban diferente aspecto macroscópico, y diferentes rasgos histológicos y perfiles inmunohistoquímicos, correspondientes a fibrotecomas y adenocarcinomas serosos papilares bilaterales de alto grado en colisión. A pesar de la quimioterapia aplicada, la condición condujo a un resultado fatal para la paciente, casi un año después de realizada la cirugía. Los tumores ováricos bilaterales plantean la cuestión de si se trata de tumores primarios o metástasis. La ocurrencia bilateral simultánea de tumores epiteliales superficiales con otros tipos de tumores ováricos es rara, y por tanto, plantea un gran desafío a la hora de realizar un diagnóstico diferencial adecuado.


Subject(s)
Humans , Female , Middle Aged , Ovarian Neoplasms/diagnosis , Thecoma/diagnosis , Adenocarcinoma/diagnosis , Immunohistochemistry , Fatal Outcome
10.
Korean Journal of Family Medicine ; : 307-313, 2019.
Article in English | WPRIM | ID: wpr-759826

ABSTRACT

BACKGROUND: Cancer survivors are at a higher risk of primary cancer recurrence and development of second primary cancer. In both cases, early disease detection is crucial. This cross-sectional study assessed cancer screening participation rates according to cancer history. METHODS: Data were obtained from the 2010–2012 Korea National Health and Nutrition Examination Survey for 12,500 participants. Of these, 624 cancer survivors were enrolled in this study. Sampling weights were applied to maintain the representativeness of the Korean adult population. RESULTS: Overall 2-year cancer screening rates prior to the survey in male and female cancer survivors were 59.9% and 73.7%, respectively, while opportunistic cancer screening rates were 33.5% and 52.1%, respectively. The odds ratios (95% confidence interval) of the overall cancer screening among the cancer survivors, compared to others, were 1.16 (0.79–1.72) in male and 1.78 (1.20–2.63) in female participants, after the adjustment for confounding variables. The odds ratios (95% confidence interval) for opportunistic cancer screening and National Cancer Screening Program among cancer survivors were 1.56 (1.07–2.27) and 0.80 (0.53–1.21) in males and 2.05 (1.46–2.88) and 0.66 (0.46–0.95) in females. CONCLUSION: Female cancer survivors showed a higher rate of overall and opportunistic cancer screening than did the male cancer survivors. Further efforts are required to improve cancer screening among male cancer survivors.


Subject(s)
Adult , Female , Humans , Male , Cross-Sectional Studies , Diagnosis , Early Detection of Cancer , Korea , Mass Screening , Neoplasms, Second Primary , Nutrition Surveys , Odds Ratio , Recurrence , Survivors , Weights and Measures
11.
Journal of Cancer Prevention ; : 48-53, 2019.
Article in English | WPRIM | ID: wpr-764295

ABSTRACT

BACKGROUND: The National Lung Screening Trial (NLST) and NELSON trial showed that low-dose chest computed tomography (LDCT) screening significantly reduced the mortality form lung cancer. Although cancer survivors are known to have high risk for second malignant neoplasm (SMN), the usefulness of LDCT screening for lung cancer in cancer survivors is not clear. METHODS: Between August 2016 and August 2017, 633 long-term colorectal cancer (CRC) survivors visited the survivorship clinic in Cancer Prevention Center, Yonsei Cancer Center, Seoul, Republic of Korea. We surveyed the smoking status and recommended LDCT screening to ever-smoking CRC survivors aged 55–80 years. The participants were classified into three risk groups: risk group 1 (RG1) who met the NLST criteria (Age 55–74 years, ≥ 30 pack-years of smoking, smoking cessation < 15 years); risk group 2 (RG2) who would not meet the NLST criteria but were at increased 6-year risk of lung cancer (PLCOM2012 ≥ 0.0151); risk group 3 (RG3) who did not meet any of the criteria above. RESULTS: Among 176 ever-smoking CRC survivors, 173 (98.3%) were male, 32 (18.2%) were current-smoker, and median age was 66 years (range, 55–79 years). We found 38 positive findings (non-calcified nodule ≥ 4 mm), 8 clinically significant findings, 66 minor abnormalities, and 64 negative findings on LDCT. Positive findings were identified in 15 of 79 (19.0%) of RG1, in 9 of 36 (25%) of RG2, and in 14 of 61 (23.0%) of RG3. Second primary lung cancers were found in 2 patients of RG2, and in 1 patient of RG3. SMN was most frequently found in RG2 (11 of 36 patients, 30.6%), compared with RG1 (12.7%) or RG3 (9.8%) (P = 0.016). CONCLUSIONS: LDCT screening for lung cancer in Korean CRC survivors is feasible. Well-designed clinical trial for defining high risk patients for lung cancer among CRC survivors is needed.


Subject(s)
Humans , Male , Colorectal Neoplasms , Early Detection of Cancer , Lung Neoplasms , Lung , Mass Screening , Mortality , Neoplasms, Second Primary , Republic of Korea , Seoul , Smoke , Smoking , Smoking Cessation , Survival Rate , Survivors , Thorax
12.
CorSalud ; 10(4): 330-335, oct.-dic. 2018. graf
Article in Spanish | LILACS | ID: biblio-1089699

ABSTRACT

RESUMEN La asociación de dos tumores de diferente origen en un mismo paciente es cada vez más frecuente en la práctica clínica actual. Se presenta un caso con una rara asociación de mixoma cardíaco e hipernefroma, previamente tratado. Ante la presencia de manifestaciones neurológicas, inicialmente se planteó el diagnóstico de metástasis cerebral del tumor renal; luego, con el hallazgo ecocardiográfico de una masa intracardíaca, se pensó en la posibilidad de trombo, por lo que se decidió practicar cirugía cardíaca con carácter urgente para resecarla. El estudio anatomopatológico confirmó la existencia de un mixoma cardíaco, por lo que se trata de un enfermo con dos enfermedades tumorales cuya coincidencia ha sido pocas veces descrita.


ABSTRACT The association of two tumors of different origin in the same patient is becoming more frequent in the current clinical practice. Here is presented a case with a rare association of cardiac myxoma and hypernephroma, previously treated. Due to the presence of neurological symptoms, there was initially set a diagnosis of brain metastasis from the renal tumor; then, with the echocardiographic finding of an intracardiac mass, the possibility of thrombus was considered, therefore a cardiac surgery was decided to be performed urgently in order to resect it. The pathologic examination confirmed the existence of a cardiac myxoma, then, we have a patient with two tumor diseases whose coincidence has been rarely described.


Subject(s)
Myxoma , Carcinoma, Renal Cell , Embolism , Neoplasms, Multiple Primary
13.
Int. j. odontostomatol. (Print) ; 12(2): 125-130, jun. 2018. tab, graf
Article in English | LILACS | ID: biblio-954253

ABSTRACT

ABSTRACT: Multiple salivary gland tumors represent an unusual event characterized by the development of composite lesions originated from minor or major salivary glands. These neoplasms can be categorized into three perspectives: Histologic type, time of appearance and topographic distribution. We report an unusual case of a 73-year-old black man with an acinic cell carcinoma (ACC) of the oral mucosa discovered incidentally during surgical removal of an adjacent mucocele. Approximately one year after the first consultation, the patient was seen at the local cancer reference center with a third lesion that was diagnosed as an adenoid cystic carcinoma (AdCC) of the upper lip. The patient underwent surgical reconstruction of the treated areas and has been free of the disease for the past year. To our knowledge, the combination of ACC and AdCC in intraoral sites has not been reported in the literature.


RESUMEN: Los tumores de glándulas salivales múltiples representan un evento inusual caracterizado por el desarrollo de lesiones compuestas, originadas en glándulas salivales menores o mayores. Estos neoplasmas se pueden categorizar en tres perspectivas: tipo histológico, tiempo de aparición y distribución topográfica. Reportamos un caso inusual de un hombre negro de 73 años con un carcinoma de célula acínica (ACC) de la mucosa oral descubierta incidentalmente durante la extirpación quirúrgica de un mucocele adyacente. Aproximadamente un año después de la primera consulta, el paciente se presentó en el centro de referencia del cáncer local con una tercera lesión que fue diagnosticada como carcinoma adenoide quístico (AdCC) del labio superior. El paciente se sometió a la reconstrucción quirúrgica de las áreas tratadas y durante el último año no ha presentado recurrencia de la enfermedad. De acuerdo a nuestro conocimiento la combinación de ACC y AdCC en sitios intraorales no se ha informado en la literatura.


Subject(s)
Humans , Male , Aged , Salivary Gland Neoplasms/pathology , Neoplasms, Second Primary/mortality , Carcinoma, Acinar Cell/pathology , Carcinoma, Adenoid Cystic/surgery , Radiotherapy , Biopsy , Salivary Gland Neoplasms/therapy , Carcinoma, Acinar Cell/therapy , Lip
14.
Cancer Research and Treatment ; : 293-301, 2018.
Article in English | WPRIM | ID: wpr-739607

ABSTRACT

PURPOSE: Secondary primary cancers (SPCs) commonly arise in patients with renal cell carcinoma (RCC). We designed the present study to estimate the SPC incidence in Korean patients with RCC. MATERIALS AND METHODS: The study cohort was population-based and consisted of 40,347 individuals from the Korean Central Cancer Registry who were diagnosed with primary renal cancer between 1993 and 2013. Standardized incidence ratios (SIRs) for SPCs were estimated for different ages at diagnosis, latencies, diagnostic periods, and treatments. RESULTS: For patients with primary RCC, the risk of developing a SPC was higher than the risk of developing cancer in the general population (SIR, 1.13; 95% confidence interval, 1.08 to 1.18). Most cancer types showed higher incidences in patients with RCC than in the general population. However, the relative incidence of gastric cancer as an SPC varied by age. Gastric cancer incidence was elevated in young patients (< 30 years) with RCC, but reduced in older (≥ 30) patients with RCC. Patients with advanced RCC died prematurely, regardless of SPC development. In contrast, those with early-stage RCC survived for longer periods, although SPC development affected their post-RCC survival. After SPC development, women had better survival than men. CONCLUSION: In Korean patients with primary RCC, the incidence of SPC was 13% higher than the incidence of cancer in the general population. These findings may play important roles in the conduct of follow-up evaluations and education for patients with RCC.


Subject(s)
Female , Humans , Male , Carcinoma, Renal Cell , Cohort Studies , Diagnosis , Education , Follow-Up Studies , Incidence , Kidney Neoplasms , Kidney , Korea , Neoplasms, Second Primary , Prognosis , Stomach Neoplasms
15.
Cancer Research and Treatment ; : 1175-1185, 2018.
Article in English | WPRIM | ID: wpr-717750

ABSTRACT

PURPOSE: Pancreatic cancer associated double primary tumors are rare and their clinicopathologic characteristics are not well elucidated. MATERIALS AND METHODS: Clinicopathologic factors of 1,352 primary pancreatic cancers with or without associated double primary tumors were evaluated. RESULTS: Of resected primary pancreatic cancers, 113 (8.4%) had associated double primary tumors, including 26 stomach, 25 colorectal, 18 lung, and 13 thyroid cancers. The median interval between the diagnoses of pancreatic cancer and associated double primary tumors was 0.5 months. Overall survival (OS) of pancreatic cancer patients with associated double primary tumors was longer than those with pancreatic cancer only (median, 23.1 months vs. 17.0 months; p=0.002). Patients whose pancreatic cancers were resected before the diagnosis of metachronous tumors had a better OS than patients whose pancreatic cancer resected after the diagnosis of metachronous tumors (48.9 months and 13.5 months, p=0.001) or those whose pancreatic cancers were resected synchronously with non-pancreas tumors (19.1 months, p=0.043). The OS of pancreatic cancer patients with stomach (33.9 months, p=0.032) and thyroid (117.8 months, p=0.049) cancers was significantly better than those with pancreas cancer only (17.0 months). CONCLUSION: About 8% of resected pancreatic cancers had associated double primary tumors, and those from the colorectum, stomach, lung, and thyroid were common. Patients whose pancreatic cancer was resected before the diagnosis of metachronous tumors had better OS than those resected after the diagnosis of metachronous tumors or those resected synchronously.


Subject(s)
Humans , Diagnosis , Lung , Neoplasms, Multiple Primary , Neoplasms, Second Primary , Pancreas , Pancreatic Neoplasms , Prognosis , Stomach , Thyroid Gland , Thyroid Neoplasms
16.
Cancer Research and Treatment ; : 428-435, 2018.
Article in English | WPRIM | ID: wpr-714229

ABSTRACT

PURPOSE: Previous western studies have found Caucasians with skin cancer, either melanoma or nonmelanoma skin cancer (NMSC), have an elevated risk of second primary cancer. Our objective was to assess the risk of second primary cancer in Taiwanese with NMSC. MATERIALS AND METHODS: By using data from Taiwan's National Health Insurance Research Database, we conducted a population-based cohort study to assess the risk of incident second primary cancer in Taiwanese affected by NMSC. RESULTS: We identified 505 subjects with NMSC and 2,020 matched controls. After adjustment for potential confounders including age, sex, urbanization, and Charlson Comorbidity Index, people who had NMSC had a 1.43-fold (95% confidence interval [CI], 1.05 to 1.96) risk for the development of second primary cancer as comparedwith control group. Menwith NMSC had a 2.99-fold (95% CI, 1.00 to 9.10) risk for second primary cancer involving the lip, oral cavity, and pharynx and a 3.51-fold (95% CI, 1.21 to 10.17) risk for second primary cancer involving the genitourinary organs when compared to the control group. By contrast, women with NMSC did not have an increased risk of second primary cancer. CONCLUSION: This study revealed Asians with NMSC have an increased risk of second primary cancer. Our findings can be a useful reference for health care for people diagnosed with NMSC.


Subject(s)
Female , Humans , Asian People , Cohort Studies , Comorbidity , Delivery of Health Care , Lip , Melanoma , Mouth , National Health Programs , Neoplasms, Second Primary , Pharynx , Skin Neoplasms , Skin , Urbanization
17.
Korean Journal of Otolaryngology - Head and Neck Surgery ; : 217-222, 2018.
Article in Korean | WPRIM | ID: wpr-713852

ABSTRACT

Multiple primary malignant neoplasms indicate an occurrence of two or more malignancies in a patient, and double primary cancers are the most common type. When the second primary cancer occurs simultaneously or within 6 months after the first primary cancer is diagnosed, it is called synchronous carcinoma. If the second primary cancer occurs after 6 months, it is defined as metachronous carcinoma. Recently, we experienced a patient who was diagnosed as double primary cancer in the nasopharynx and nasal cavity. The tumors occurred simultaneously and histopathological examinations revealed nasopharyngeal nonkeratinizing carcinoma in the right nasopharynx and extranodal NK/T-cell lymphoma in the left nasal cavity (inferior turbinate). In situ hybridization showed positivity for Epstein-Barr virus, which encoded early RNA in the neoplastic cells of both specimens. We present this rare disease entity with a review of the relevant literature and a survey of the clinical characteristics.


Subject(s)
Humans , Herpesvirus 4, Human , In Situ Hybridization , Lymphoma , Nasal Cavity , Nasopharynx , Neoplasms, Multiple Primary , Neoplasms, Second Primary , Rare Diseases , RNA
18.
Journal of Breast Cancer ; : 62-69, 2018.
Article in English | WPRIM | ID: wpr-713696

ABSTRACT

PURPOSE: Breast cancer is one of the most common malignancies worldwide and the second most common cancer among Korean women. The prognosis of breast cancer is poor in patients with other primary cancers. However, there have been few clinical studies regarding this issue. Therefore, we analyzed the characteristics and prognosis of patients with breast cancer with multiple primary cancers (MPCs). METHODS: Data from the Korean Breast Cancer Society Registry were analyzed. Data from enrolled patients who underwent surgery for breast cancer were analyzed for differences in prognosis dependent on the presence of MPCs, and which MPC characteristics affected their prognosis. RESULTS: Among the 41,841 patients analyzed, 913 patients were found to have MPCs, accounting for 950 total MPCs. There was a significant difference in survival rates between the breast cancer only group and the MPC group. The 5-year survival rates were 93.6% and 86.7% and the 10-year survival rates were 87.5% and 70.4%, respectively. Among the 913 patients with MPCs, patients with two or more MPCs had significantly worse prognoses than patients with a single MPC. With respect to the time interval between breast cancer and MPC occurrence, patients with a 5-year or greater interval had significantly better prognoses than patients with less than 1 year between occurrences. Among MPCs, thyroid cancer was the most common primary cancer. However, this type was not related to the prognosis of breast cancer. Gynecologic cancer, colorectal cancer, upper gastrointestinal cancer, and lung cancer were related to breast cancer prognosis. CONCLUSION: MPCs were a poor prognostic factor for patients with breast cancer. Two or more MPCs and a shorter time interval between occurrences were worse prognostic factors. Although MPCs were a poor prognostic factor, thyroid cancer did not affect the prognosis of patients with breast cancer.


Subject(s)
Female , Humans , Breast Neoplasms , Breast , Colorectal Neoplasms , Gastrointestinal Neoplasms , Lung Neoplasms , Neoplasms, Multiple Primary , Prognosis , Survival Rate , Thyroid Neoplasms
19.
Korean Journal of Clinical Oncology ; (2): 83-88, 2018.
Article in English | WPRIM | ID: wpr-788041

ABSTRACT

PURPOSE: Double primary colorectal cancer (CRC) and gastric cancer (GC) represent the most common multiple primary malignant tumors (MPMT) in Korea. The recognition and screening of hidden malignancies other than the primary cancer are critical. This study aimed to investigate the clinicopathologic characteristics and survival rates in patients with synchronous or metachronous double primary CRC and GC.METHODS: Between January 1994 and May 2018, 11,050 patients were diagnosed with CRC (n=5,454) or GC (n=5,596) at Gil Medical Center. MPMT and metastatic malignant tumors were excluded from this study. A total of 103 patients with double primary CRC and GC were divided into two groups: the synchronous group (n=40) and the metachronous group (n=63). The incidence, clinicopathologic characteristics, and survival rate of the two groups were analyzed.RESULTS: The incidence of synchronous and metachronous double primary CRC and GC was 0.93%. Double primary CRC and GC commonly occurred in male patients aged over 60 years with low comorbidities and minimal previous cancer history. There were significant differences between the synchronous and metachronous groups in terms of age, morbidity, and overall survival. Metachronous group patients were 6 years younger on average (P=0.009), had low comorbidities (P=0.008), and showed a higher 5-year overall survival rate (94.8% and 61.3%, P < 0.001) in contrast to synchronous group.CONCLUSION: When primary cancer (CRC or GC) is detected, it is important to be aware of the possibility of the second primary cancer (GC or CRC) development at that time or during follow-up to achieve early detection and better prognosis.


Subject(s)
Humans , Male , Colorectal Neoplasms , Comorbidity , Follow-Up Studies , Incidence , Korea , Mass Screening , Neoplasms, Multiple Primary , Neoplasms, Second Primary , Prognosis , Stomach Neoplasms , Survival Rate
20.
Rev. colomb. cir ; 32(4): 304-318, 2017. fig, tab
Article in Spanish | LILACS, COLNAL | ID: biblio-905249

ABSTRACT

El cáncer colorrectal con metástasis a hígado es una enfermedad frecuente que hasta hace pocos años se consideraba únicamente de tratamiento paliativo. Sin embargo, con la reciente aparición de nuevas técnicas y avances para aumentar la posibilidad de resecar las lesiones y los nuevos esquemas de quimioterapia, se ha logrado la resección quirúrgica de este tipo de lesiones, extrayendo todo el tejido tumoral macroscópico e impactando de forma positiva la supervivencia de estos pacientes. Múltiples esquemas se han propuesto para el tratamiento de las lesiones sincrónicas con el fin de mejorar la supervivencia de los pacientes. Si bien no hay consenso sobre cuál es el mejor esquema terapéutico en estos casos, parece ser que lo más importante es que se logre completar de manera exitosa el esquema elegido. En general, la tendencia actual es practicar las intervenciones quirúrgicas del hígado primero, a menos que el tumor primario se encuentre sintomático; en este caso, la colectomía es el abordaje inicial. Las resecciones simultáneas hacen parte del arsenal terapéutico de estos pacientes. Múltiples grupos sugieren no asociar una resección de recto bajo a una hepatectomía mayor. Por su parte, las lesiones metacrónicas deben resecarse según el tamaño y la posibilidad de resección una vez hecho el diagnóstico. Es importante tener en cuenta que, aunque se logre una resección completa del tejido tumoral con márgenes R0 , las recurrencias son frecuentes debido a que la diseminación tumoral microscópica ya está presente; por esta razón, es indispensable agregar la quimioterapia para mejorar el pronóstico de los pacientes


Metastatic colorectal cancer in the liver is a frequent pathology that until a few years ago was considered only for palliative management. However, with the recent advent of new techniques and advances to improve the resectability of such lesions and the new schemes of chemotherapy, oncological resection of these lesions can be performed, extracting all macroscopic tumor and achieving a positive impact on patient´s survival. Multiple schemes have been postulated for the management of synchronous lesions in order to improve patient survival, although there is no consensus about which is the best scheme in these cases; it seems that the most important factor is to complete successfully the proposed scheme. In general, the current trend is to perform the liver resection first unless the primary tumor is symptomatic, in which case a colectomy should be performed as the initial approach. Simultaneous resections are part of the therapeutic arsenal in these patients. Many groups suggest not to associate a low rectal resection with a major hepatectomy. On the other hand, metachronic lesions should be resected based on their size and the possibility of resection should be considered once the diagnosis has been made. It is important to take into account that even if a complete resection of the tumor and R0 margins are achieved, recurrences are frequent because microscopic tumor dissemination is already present; therefore, the addition of chemotherapy regimens should be mandatory to Improve the oncological prognosis of these patients


Subject(s)
Humans , Neoplasms, Second Primary , Clinical Protocols , Colonic Neoplasms , Neoplasm Metastasis
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