Quistes mesoteliales benignos con posible origen en las trompas de Falopio resecados por laparotomía / Benign mesothelial cysts with possible origin in the Fallopian tubes resected by laparotomy

Introducción. Los quistes mesoteliales benignos son una entidad poco frecuente, que ocurren especialmente en mujeres en edad reproductiva. Se deben a una proliferación anómala del mesotelio que puede ser originada en varias estructuras intraabdominales e inicialmente es asintomática. Caso clínico. Se presenta el caso de una mujer de 20 años con un cuadro sugestivo de neoplasia maligna, en quien se confirmó el diagnóstico de quiste mesotelial originado en la trompa de Falopio derecha. Se realizó tratamiento quirúrgico exitoso. Discusión. A pesar de la estrecha relación de esta entidad con el útero y los ovarios, no se encuentran reportes de quistes mesoteliales originados a partir de las trompas de Falopio. El tratamiento de los quistes mesoteliales es quirúrgico y en el caso de esta paciente se hizo con la finalidad de mejorar los síntomas y erradicar la enfermedad. Las decisiones fueron tomadas basadas en la opinión de expertos en oncología en una junta de tumores gastrointestinales. Conclusiones. Los quistes mesoteliales son neoplasias de baja incidencia, pero se deben tener en cuenta como diagnóstico diferencial de los tumores abdominales. Se presenta el caso de una paciente tratada de forma quirúrgica con resultados exitosos y seguimiento a un año sin recurrencias

Introduction. Benign mesothelial cysts (BMC) are a rare entity that occurs especially in women of reproductive age. It is due to an abnormal proliferation of the mesothelium that can originate from various intra-abdominal structures and it is initially asymptomatic. Clinical case. This is a case of a 20-year-old woman with a suspicious malignant neoplasia, in whom the diagnosis of a mesothelial cyst originating in the right Fallopian tube was confirmed. Successful surgical treatment was achieved. Discussion. Despite the close relationship of this entity with the uterus and ovaries, there are no reports of me-sothelial cysts originating from the Fallopian tubes. The treatment of mesothelial cysts is surgical and in the case of this patient it was performed in order to improve the symptoms and eradicate the disease. The decisions were taken based on the oncologists' expert opinion of the gastrointestinal tumor board. Conclusions. Mesothelial cysts are neoplasms of low incidence, but they should be considered as a differential diagnosis of abdominal tumors. The case of a patient treated surgically with successful results and a one-year follow-up without recurrences is presented

Mesotelioma peritoneal multiquístico benigno: reporte de un caso y revisión de la literatura / Benign multicystic peritoneal mesothelioma: case report and literature review

INTRODUCCIÓN: El mesotelioma peritoneal multiquístico benigno (MPMB) es una entidad con muy baja incidencia que se presentan con mayor frecuencia en mujeres jóvenes. CASO CLÍNICO: Paciente de 17 años que consulta por amenorrea secundaria. Además, refería pérdida de peso, estreñimiento y molestias abdominales. La exploración fue normal y en las pruebas de imagen se objetivó una pelvis ocupada por una masa multiquística, de unos 20 cm de diámetro máximo, de paredes finas y contenido anecoico. Se solicitaron marcadores tumorales de los cuales sólo se encontró elevado el CA 19.9 (35,2 U/mL). Se decidió realizar una laparoscopia exploradora para establecer un diagnóstico y ante los hallazgos y al considerarse la masa fácilmente resecable, en el mismo acto quirúrgico se extirpó por completo para su estudio anatomopatológico, que confirmó un MPMB. Se desestimaron tratamientos adicionales y actualmente se encuentra en seguimiento y asintomática. CONCLUSIÓN: La patogénesis del MPMB no está clara. Algunos autores defienden que se trata de una reacción peritoneal a un daño inflamatorio, otros apoyan que se trata de una neoplasia benigna. Esta naturaleza incierta, junto con la escasa experiencia, hacen que el manejo resulte complejo. Es necesario individualizar cada caso e intentar ser conservadores especialmente en pacientes jóvenes. Si se opta por un manejo activo, lo más acertado es la citorreducción completa seguida de quimioterapia hipertérmica peritoneal. El seguimiento, en cualquier caso, debe ser exhaustivo y multidisciplinar principalmente con pruebas de imagen.

BACKGROUND: Benign Multicystic Peritoneal Mesothelioma (BMPM) is an entity with a very low incidence that occurs more frequently in young women. CASE REPORT: A 17-year-old woman attended for secondary amenorrhea. She also referred to weight loss, constipation and abdominal discomfort. The examination was normal and echography revealed a pelvis occupied by a 20 centimeters multicystic mass, with thin walls and anechoic content. A preoperative study with tumor markers was requested in which only a CA 19.9 elevation was observed (35.2 U/ml 0-27). It was decided to perform an exploratory laparoscopy to establish a diagnosis. Due to the findings and because of the fact that the mass was considered easy to remove, it was completely removed in the same surgical act. The pathological result confirmed a BMPM. Additional treatments have been dismissed and are the patient is currently being followed up without symptoms. CONCLUSION: The pathogenesis of BMPM is unclear. Some authors argue that it is a peritoneal reaction to inflammatory damage, others support that it is a benign neoplasm. This uncertain nature coupled with limited experience make management complex. It is necessary to evaluate each case and try to be conservative especially in young patients. If surgery management is chosen, complete cytoreduction followed by hyperthermic peritoneal chemotherapy is the most successful option. The follow-up in any case must be exhaustive and multidisciplinary, mainly with imaging tests.

Benign multicystic peritoneal mesothelioma: literature review and update

Benign multicystic peritoneal mesothelioma (BMPM) is a rare peritoneal tumor diagnosed predominantly in pre-menopausal women. Associated risk factors include endometriosis and pelvic inflammatory disease in women, and prior abdominal surgery in both genders. To date, the pathogenesis of this disease remains controversial with possible etiologies, including a neoplastic versus a reactive process. Given the risk factors, some authors believe that this disease is secondary to a reactive process. However, because some studies describe cases where there is no prior surgical history or inflammatory milieu present, and because of this entity's predilection for recurrence, some authors believe the origin to be neoplastic. Some genetic and familial associations have also been reported. Malignant transformation is extremely rare, with only two cases reported in the literature, despite the recurrence potential. Like the etiology, the name of this entity is also controversial. Some authors prefer the term "peritoneal inclusion cyst (PCM)" instead of "benign cystic mesothelioma" and argue that the term mesothelioma should only be used when there is evidence of atypia. Most cases of BMPM are discovered incidentally. Others reflect sequela of tumor mass effect. It appears intra-operatively as large, multi-focal, cystic lesions in the peritoneal and pelvic cavity. Diagnosis is achieved through surgical sampling with histopathological examination. Immunobiologically, BMPM exhibits multiple small cystic spaces with flattened lining containing calretinin positive cells without atypical features, mitotic figures, or tissue invasion. Treatment includes cytoreductive surgery. Here we present a case of BMPM in a 60-year-old male - a rare disease in an uncommon patient population.

Mesotelioma benigno como causa de dolor abdominal inespecífico en un paciente con Enfermedad de Crohn / Benign multicystic peritoneal mesothelioma in a patient with Crohn disease

Benign multicystic peritoneal mesothelioma is an uncommon lesion arising from the peritoneal mesothelium. It is asymptomatic or presents with unspecific symptoms. Imaging techniques may reveal it, however the final diagnosis can only be made by histopathology. Surgery is the only effective treatment considering its high recurrence rate. We report a 19 years old male with Crohn’s disease. Due to persistent abdominal pain, an abdominal magnetic resonance imaging was performed, showing a complex cystic mass in the lower abdomen. The patient underwent surgery and the lesion was completely resected. The pathological study reported a benign multicystic peritoneal mesothelioma.

Complicated benign cystic mesothelioma of mesoappendix misdiagnosed as an appendiceal abscess in a postpartum period woman

Benign cystic mesothelioma is an uncommon tumor arising from the peritoneal mesothelium. It is characterized by multilocular grapelike, thin-, and translucent-walled cysts, or a unilocular cyst lined by benign mesothelial cells. It occurs predominantly in women of reproductive age, and shows a predilection for the surface of the pelvic peritoneum or visceral peritoneum. Patients usually present abdominal pain and palpable mass, but many cases have been found incidentally during laparotomy. Definite preoperative diagnosis is known to be difficult. Benign cystic mesothelioma has a tendency towards local recurrence, although the gross microscopic features are benign. Moreover, there is controversy over whether this disease is neoplastic or reactive. Initial complete surgical resection and cytoreductive surgery for recurred cases are standard treatments. In the following report, we describe a case of complicated benign cystic mesothelioma in a postpartum woman, involving the pelvic peritoneum and mesoappendix, which was initially misdiagnosed as a periappendiceal abscess.

Quiste mesotelial simple gigante / Giant simple mesothelial CYST

El quiste mesotelial simple es una rara causa de quistes mesentéricos. El tamaño de estas lesiones suele ser de pocos centímetros y por tanto suele ser asintomático siendo su diagnóstico un hallazgo imagenológico o intraoperatorio. Caso clínico: Se documenta el caso de una mujer de 40 años de edad quien presenta un quiste mesotelial simple de gran tamaño y sintomático el cual fue manejado mediante resección quirúrgica completa sien-do este el tratamiento de elección. El comportamiento clínico sintomático, tener el antecedente de cirugías pelvianas y las dimensiones del tumor, hacen pensar en un mesotelioma quístico benigno. Sin embargo, el carácter unilocular permite catalogarlo como un quiste mesotelial simple. La diferenciación entre ambas lesiones no es meramente académica pues el mesotelioma quístico benigno tiene una recidiva alta y puede incluso malignizarse(AU)

The simple mesothelial cyst is a rare cause of the mesenteric cysts. The size of this lessons are usually of a few centimeters andasymptomatic so the diagnosis is based on imaging studies orintra operatory findings. Clinical case: We report a female patient of 40 years old who had a simple mesothelial cyst of big size andsymptomatic, which was managed by a complete surgical excision, being this method the treatment of choice. The symptoms that thepatient described, the previous pelvic surgery and the tumor dimensions had the characteristics of a benign cystic mesothelioma. However, the unilocular characteristic allow to categorize it like asimple mesothelial cyst. The differentiation between both lessonsis not academic due to the fact that the benign cyst mesotheliomahas a high relapse and even could become a malignant lesson(AU)

Multicystic peritoneal mesothelioma: not always a benign disease

Mesothelioma is a slow-growing insidious lesion of neoplastic aetiology arising from the pleural, peritoneal or pericardial mesothelium. It shows a predilection for the surfaces of the pelvic viscera and has a high rate of recurrence after excision. Cystic mesotheliomas are not associated with asbestos exposure. We report a case of cystic mesothelioma of the peritoneum encasing the ovary, which presented as a cystic adnexal mass. As highlighted in this case and other recent reports, a cystic mesothelioma should not be referred to as a benign cystic mesothelioma, as it has potential for locoregional invasion, as well as distant nodal and serosal metastases. This tumour should be treated with aggressive cytoreductive surgery and appropriate chemotherapy. We review the differential diagnosis of this rare entity and suggest guidelines for its differentiation.

Mesotelioma maligno difuso primario de peritoneo / Primary diffuse malignant peritoneal mesothelioma

El mesotelioma peritoneal maligno es una neoplasia de presentación infrecuente, de curso insidioso, sintomática y de presentación poco específica en fase avanzada, de difícil diagnóstico y alta letalidad. Es la neoplasia más común de la serosa peritoneal, ocupando el segundo lugar de localización de los mesoteliomas, después del mesotelioma pleural. Es más frecuente en hombres, en mayores de 60 años y se ha relacionado en un 80% a la exposición crónica al asbesto. Generalmente su primera manifestación es ascitis, que se acompaña de dolor abdominal, astenia, hiporexia y pérdida de peso. Se puede diagnosticar a través del estudio histológico e inmunohistoquímico de líquido ascítico, biopsia peritoneal, y como métodos complementarios, TC de Abdomen y CT-PET. Presentamos el caso de un paciente masculino de 70 años de edad, con antecedente de adenocarcinoma prostático tratado con radioterapia y bloqueo hormonal, en remisión, Cardiopatía Isquémica e Hipertensiva en condición post-Bypass coronario, quien consulta por disnea, ascitis, hiporexia, astenia, con evidencia de líquido ascítico hemorrágico y GASA de bajo gradiente.

Malignant peritoneal mesothelioma is an infrequent neoplasm, of insidious course, symptomatic presentation and usually is diagnosed at an advanced stage diagnosis. It is the most common malignancy of the peritoneum and the the second location of mesothelioma, preceded by pleural mesothelioma. It is more common in men older than 60 year sand has been linked in 80% to chronic exposure to asbestos. Usually ascites, abdominal pain, fatigue, decreased appetite and weight loss are the first signs. It can be diagnosed through histological and immunohistochemical study of ascitic fluid, peritoneal biopsy, abdominal CT and CT-PET. We report the case of a male patient. 70 years with a history of heart disease and prostatic carcinoma treated with radiotherapy and immunosupressive therapy, who consults with dyspnea, ascites, hyporexia, fatigue and evidence of hemorrhagic ascites.

Quiste mesotelial simple gigante abdomino-pélvico / Giant pelvic and abdominal omental cyst: report of one case

Se presenta el caso de una mujer de 41 años que consulta por dolor abdominal y pelviano de carácter sordo de 6 semanas de evolución sin compromiso del estado general. Refiere el antecedente de una histerectomía por mioma realizada hace 3 años. La ecotomografía y la TAC de abdomen y pelvis revelan una lesión quística gigante de 15 x 8 x 12 cm que ocupa parte del abdomen y la pelvis. Luego de una resección parcial y marsupialización es referida a cirugía por recidiva precoz del tumor quístico. Es reintervenida, lográndose una extirpación completa más anexectomía bilateral con buena evolución posterior. El estudio histopatológico confirma el diagnóstico inicial de quiste mesotelial simple. La ubicación pelviana de la lesión, el comportamiento clínico (recidiva precoz con crecimiento rápido) y las dimensiones son más característicos de un mesotelioma quístico benigno. Sin embargo, el carácter unilocular permite catalogarlo como un quiste mesotelial de crecimiento excepcional. La distinción entre ambas entidades no es menor, toda vez que el mesotelioma quístico benigno tiene una recidiva alta y puede malignizarse.

We report a 41 years old women presenting with abdominal and pelvic pain lasting six weeks. She had a history of hysterectomy three years ago. Abdominal ultrasound and CAT scan showed a giant cystic lesion of 15 x 8 x 12 cm that occupied a great portion of the abdomen and pelvis. After a partial resection and marsupialization, she was refereed to surgery due to an early relapse of the cyst. She was operated again, performing a complete cyst excision and bilateral anexectomy, with a good postoperative evolution. Pathology confirmed the diagnosis of a simple omental cyst. The unilocular feature of the lesion is characteristic of omental cysts. However, due to the pelvic location and dimensions, the differential diagnosis must be made with benign cystic mesothelioma, that had a high rate of relapse and may become malignant.

Benign mesothelioma of peritoneum presenting as a pelvic mass

A large solitary multiloculated pelvic cyst in a 40-year-old woman with chronic pelvic pain was diagnosed to be a Multicystic Benign Mesothelioma [MBM] of peritoneum at laparotomy. Operative findings showed dense adhesions between uterus and bladder anteriorly, small intestines and pouch of Douglas posteriorly, a right ovarian cyst cm containing clear serous fluid and two nodular deposits were seen in the pouch of Douglas, small multiple deposits was found over the mesentery of small intestine and parietal peritoneum. Total abdominal hysterectomy with bilateral oophorectomy and infracolic omentectomy was done. During surgery, there was injury to the small intestine hence, resection of 10 inches of small intestine with re-anastomosis was carried out. Postoperative recovery was satisfactory. At 3 years follow-up, patient is symptom-free

Multilocular peritoneal inclusion cyst--a case report.

Multilocular Peritoneal Inclusion Cyst (MPIC) is a rare mesothelial lesion. It is most commonly found in women of reproductive age group involving the abdominal and pelvic peritoneum. Previously, this lesion was often confused with cystic lymphangioma, but now its mesothelial origin has been confirmed. We report a case of a 26-year old female who underwent Caesarean section during which cysts which were multiloculated, thin-walled and filled with serous fluid, were incidentally discovered. Its histopathologic examination established the diagnosis

first report of abdominal mesothelioma in a ram in Iran

Primary tumours arising from the mesothelial cells lining the peritoneal cavity, mesothelioma, have been recorded in the abdominal cavity of cattle, horses, dogs and cats. Abdominal tumour masses from a five-year-old male kordi sheep were found during routine inspection at the Mashhad abattoir. At gross examination, the tumour consisted of gray-white multiple firm, sessile nodules, approximately 2.60 kg in weight. Histopathological examination revealed numerous thin papillary projections covered by cuboidal cells with large vesicular nuclei and prominent nucleoli and in some areas the neoplastic cells lined cystic spaces. Mitotic figures were few. Based on histopathological findings, the tumour was diagnosed as abdominal mesothelioma

Benign multicystic mesothelioma of peritoneum: a clinico-pathological study of four cases

To study the clinico-pathological findings of benign multicystic mesothelioma, also known as multicystic peritoneal inclusion cyst [MPIC] which is a rare disease of mesothelial origin. the clinical medical records and the pathology reports of four patients diagnosed as having benign multicystic mesothelioma at Bahrain Defence Force Hospital during one year period between 2003-2004 were evaluated. The H and E stained slides along with the special histochemistry stains and immunoperoxidase techniques were applied for confirmation of the diagnosis. all cases in our study occurred in females aged of 28-46 years with the mean 39. Two patients had previous surgery. The chief complaints included abnormal uterine bleeding, abdominal or pelvic pain and dyspareunia. The size of the cysts ranged 2-3.2 cm in diameter. The histology showed multilocular cystic spaces lined by mesothelial cells which were confirmed by application of special stains and immunoperoxidaae techniques. benign muticystic mesothelioma/MPIC should be distinguished from other benign and malignant tumours as it has excellent prognosis if completely excised. Proper utilization of diagnostic facilities is essential for accurate diagnosis

Tumores benignos de pleura: comunicación de un caso / Benign tumors of pleur: case report

Se presenta un caso de tumor benigno localizado de la pleura en un paciente de 73 años, muy raro sobre todo a esta edad. Se señalaron los aspectos clínicos, epidemiológicos, imagenológicos, así como el pronóstico de estos tumores poco frecuentes, entre ellos el mesotelioma benigno, el cual aunque es el de mayor frecuencia presenta difícil diagnóstico preoperatorio. Se destacó la incidencia del tumor, los diferentes exámenes radiológicos y su tratamiento

Pelvic pain and dispareunia: a benign cystic mesothelioma case report

Benign cystic mesothelioma is a rare tumor originated from mesenchymal cells of the abdominal and pelvic peritoneum. This rare tumor should be considered in the differential diagnosis of young women presenting with abdominal pain and a multicystic abdominal mass

Clinical analysis of surgical management for cystic neoplasms of pancreas / 한국간담췌외과학회지

BACKGROUND: Cystic neoplasms of pancreas comprise pathologically heterogeneous groups of tumors with many shared clinical features. Although relatively uncommon, they have a very important place in the surgical pathology of the pancreas because of their high cure rate and their potential confusion with far more common pancreatic pseudocysts. METHODS: We analysed clinical features of 23 patients with pancreatic cystic neoplasm that we treated within 8-years` period (13 women, 10 men, mean age; 47.2 years old) The cystic neoplasms of pancreas comprise 5 serous cystadenoma, 3 benign mucinous cystic tumor, 3 borderline malignancy of mucinous cystic tumor and 4 mucinous cystadenocarcinoma, 4 papillary cystic tumor, 1 cystic teratoma, 1 cystic mesothelioma, 1 lymphoepithelial cyst. 1 mucinous ductal ectasia. RESULTS: Mean tumor size was 6.8cm(3 to 15cm). 73.9 percent had abdominal pain and 26.1 percent had abdominal mass. Computed tomography, ultrasonography and MRI were useful in detecting cystic mass in all cases but was not reliable to distinguish serous from mucinous tumor, benign from malignant. For the treatment of the tumor, 17 distal pancreatectomy with splenectomy, 1 distal pancreatectomy with spleen preserving, 1 proximal pancreatic resection, 2 local excision of pancreas and 1 PPPD were performed. During the period of follow up (mean: 29 months) after surgical resection, 1 recurrence occurred in the patient who underwent local excision for mucinous cystic tumor showing borderline malignancy on histologic finding. All the patients are alive except 2 patients who were lost to follow-up. CONCLUSION: Pancreatic cystic neoplasms are rare and their prognosis are acceptable when they are treated early and properly. So early detection and surgical treatment is the mainstay of management of cystic neoplasm of pancreas.

Cisto paraovariano gigante / Giant ovarian cyst

No mesossalpinge, entre a trompa e o ovário, está situado o paraovário. Os cistos paraovarianos originam-se de estruturas vestigiais de Wolff, do epitélio tubário ou de incluções peritoneais. Raramente atinguem tamanho de cisto do próprio ovário. Os autores relatam um raro caso de cisto paraovariano gigante

Benign cystic peritoneal mesothelioma in a man.

Benign cystic mesothelioma of the peritoneum is uncommon and usually occurs in women. We report this condition in a man, who was treated successfully by surgical excision of the tumor.

A Cystic Mesothelioma in the Right Colon: A case report

Cystic mesothelioma of the peritoneum is a very rare tumor which has a clinically and histologically benign nature. It occurs predominantly in young to middle-ged women and tends to recur locally. It affects chiefly the pelvic peritoneum-articularly the cul-e-ac, uterus, and rectum. We report a case of cystic mesothelioma of the visceral peritoneum which was located anterior to the ascending colon. A 54-ear-ld female patient visited our hospital with a palpable tender mass in the right flank. A computed tomographic scan of the abdomen showed a multicystic mass with an enhancing wall and septum in front of the ascending colon. The patient underwent a right hemicolectomy, and the mass was completely removed. Grossly, the tumor consisted of a multilocular cyst containing clear, serous, or gelatinous fluid and partially solid areas. Microscopically, the solid areas were composed of fibrous tissue, and the lining cells varied from flattened to cuboidal cells with a strong positive reactivity for cytokeratin and mild positive reactivity for epithelial membrane antigen on immunohistochemical staining. These findings suggest that the tumor was mesothelial in origin.

Benign Cystic Mesothelioma

Benign cystic mesothelioma (BCM) is a rare mesothelial lesion that forms multicystic masses in the upper abdomen, pelvis and retroperitoneum. Although it is categorized as a benign lesion, it has a tendency to recur. It is uncertain whether the nature of this lesion is reactive or neoplastic, but many articles support the conclusion that it is reactive rather than neoplastic. The majority of cases were associated with a history of a previous abdominal or pelvic operation, or an evidence of endometriosis or a pelvic inflammatory disease, or a combination of these findings. In a 26-year-old woman we experienced a case of BCM which was incidentally discovered at cesarean delivery revealing multilocular thin and translucent walled cysts in the pelvic cavity. Microscopic examination revealed a thin cyst wall that was composed of fibrous connective tissue and lined by internal stratified and external nonstratified single cuboidal epithelia.