scholarly journals Sclerosing Stromal Tumor of Ovary: A Case Report

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Menka Khanna ◽  
Ashish Khanna ◽  
Mridu Manjari
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Young Woman ◽  
Pelvic Pain ◽  
Malignant Tumor ◽  
Stromal Tumor ◽  
Ca 125 ◽  
Hormonal Status ◽  
Sclerosing Stromal Tumor ◽  
Sex Cord Stromal Tumor

Sclerosing stromal tumor (SST) is an extremely rare and distinctive sex cord stromal tumor which occurs predominantly in the second and third decades of life. We report a case of a 32-year-old woman who developed a sclerosing stromal tumor of ovary and presented with irregular menstruation and pelvic pain. Her hormonal status was normal but CA-125 was raised. She was suspected to have a malignant tumor on computed tomography and underwent bilateral salpingo-oopherectomy. It is therefore necessary to keep in mind the possibility of sclerosing stromal tumor in a young woman.

scholarly journals Sclerosing Stromal Tumour of Ovary- A Case Report

2016 ◽  
Vol 30 (1) ◽  
pp. 56-58
Author(s):  
Fahmida Sharmin Joty ◽  
Farhana Dewan ◽  
Fahmida Khan Lima ◽  
Bipul Biswas ◽  
Eva Rani Nondi
Keyword(s):  
Computed Tomography ◽  
Abdominal Pain ◽  
Case Report ◽  
Pelvic Pain ◽  
Malignant Tumor ◽  
Stromal Tumor ◽  
Hormonal Status ◽  
Hormonal Activity ◽  
Sclerosing Stromal Tumor ◽  
Sex Cord Stromal Tumor

Sclerosing stromal tumor (SST) is an extremely rare and distinctive sex cord stromal tumor, which occurs predominantly in the second and third decades of life. Approximately 100 cases reported since first described in 1973. It typically present with pelvic/abdominal pain and tenderness, mass, and/or abnormal menses, and with hormonal activity reported predominantly in postmenarchal females. Only 5 cases of these tumors have been reported in premenarchal girls.We report a case of a 18-year-old girl who developed a sclerosing stromal tumor of ovary and presented with excessive menstruation, pelvic pain and increased frequency of menstruation. Her hormonal status was normal. She was suspected to have a malignant tumor on computed tomography and underwent unilateral salpingo-oopherectomy. It is therefore, necessary to keep in mind the possibility of sclerosing stromal tumor in a young womanBangladesh J Obstet Gynaecol, 2015; Vol. 30(1) : 56-58

Undifferentiated-type sex cord-stromal tumor of the testis: a case report

2018 ◽  
pp. 100-103
Author(s):  
Asli Muratli ◽  
Askin Eroglu ◽  
Aysen Terzi ◽  
Ugur Mungan ◽  
Mustafa Secil
Keyword(s):  
Case Report ◽  
Stromal Tumor ◽  
Undifferentiated Type ◽  
Sex Cord Stromal Tumor

An Invasive Hemolymphangioma of the Pancreas in a Young Woman

2019 ◽  
Vol 21 (10) ◽  
pp. 798-800 ◽  
Author(s):  
Zhijun Zhang ◽  
Qinghong Ke ◽  
Weiliang Xia ◽  
Xiuming Zhang ◽  
Yan Shen ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Young Woman ◽  
Benign Tumor ◽  
Abdominal Distension ◽  
Accurate Diagnosis ◽  
Cystic Tumor ◽  
Rare Benign Tumor ◽  
Radical Surgical Resection

Background: Hemolymphangioma is a rare benign tumor. To the best of our knowledge, there were only 10 reports of this tumor of the pancreas until March 2018. Case Report: Here, we reported a large invasive hemolymphangioma of the pancreas in a young woman with a complaint of abdominal distension and an epigastric mass about 3 weeks. She was found to have a huge multilocular cystic tumor at the neck and body of pancreas on computed tomography. She was eventually diagnosed with hemolymphangioma of the pancreas after operation. After 2 years of follow-up, there was no signs of recurrence. Conclusion: From our case and literature, we can conclude that hemolymphangioma of the pancreas is uncommon benign tumor, and it is hard to make an accurate diagnosis preoperatively. Radical surgical resection should be performed whenever possible. The prognosis of this disease seems good.

SCLEROSING STROMAL TUMOR OF THE OVARY: A CASE REPORT

2003 ◽  
Vol 13 (Suppl 1) ◽  
pp. 69.4-70
Author(s):  
E. Kuscu ◽  
M. Oktem ◽  
H. Karahan ◽  
B. Bilezikci ◽  
B. Demirhan
Keyword(s):  
Case Report ◽  
Stromal Tumor ◽  
Sclerosing Stromal Tumor

Extragonadal sclerosing stromal tumor: A rare case report

2013 ◽  
Vol 40 (3) ◽  
pp. 883-886 ◽  
Author(s):  
Maral Mokhtari ◽  
Mojgan Akbarzadeh-Jahromi ◽  
Fatemeh Sari-Aslani ◽  
Bahareh Hamedi ◽  
Mandana Bagheri ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Stromal Tumor ◽  
Rare Case Report ◽  
Sclerosing Stromal Tumor

scholarly journals Pediatric Sex Cord-Stromal Tumor with Composite Morphology: A Case Report

2005 ◽  
Vol 8 (6) ◽  
pp. 680-684 ◽  
Author(s):  
Jason A. Jarzembowski ◽  
Richard W. Lieberman
Keyword(s):  
Granulosa Cell ◽  
Sertoli Cell ◽  
S100 Protein ◽  
Neuron Specific Enolase ◽  
Granulosa Cell Tumor ◽  
Cell Tumor ◽  
Stromal Tumor ◽  
Ca 125 ◽  
Sertoli Cell Tumor ◽  
Sex Cord Stromal Tumor

A 12-year-old female with developmental delay/mental retardation and a family history of gynecologic cancers presented with nonspecific abdominal complaints and was found to have a 4.5-kg, 25- x 23- x 15-cm pelvic mass with solid and cystic components and associated retro-peritoneal and mesenteric lymphadenopathy. Laboratory studies revealed increased serum levels of CA-125 and inhibin B. Histologically, the tumor exhibited several different morphologic appearances including adult granulosa cell tumor, juvenile granulosa cell tumor (with areas of marked atypia), and Sertoli cell tumor. Immunohistochemically, the tumor was positive for calretinin, MIC-2 (CD99), S100 protein, PGP 9.5, and neuron-specific enolase. Electron microscopy of the Sertoli cell tumor-like areas showed Charcot-Bottcher filaments, a distinguishing feature of Sertoli cells. Together, these findings supported a diagnosis of mixed sex cord-stromal tumor including granulosa cell tumor of adult and juvenile types and intermediate- to high-grade Sertoli cell tumor, with large areas of markedly atypical sex cord-stromal tumor.

scholarly journals Osteopoikilosis: Pain as a Presenting Symptom in Three Family Members

2011 ◽  
Vol 4 ◽  
pp. CMAMD.S7035 ◽  
Author(s):  
M.A. Aghdashi ◽  
M.M. Aghdashi ◽  
M. Rabiepoor
Keyword(s):  
Case Report ◽  
Young Woman ◽  
Pelvic Pain ◽  
Autosomal Dominant ◽  
Family Members ◽  
Familial Occurrence ◽  
Autosomal Dominant Pattern ◽  
Dominant Pattern ◽  
Radiological Examinations

Osteopoikilosis is a rare asymptomatic sclerosing bony dysplasia of benign origin. It is usually found incidentally on radiological examinations. Familial occurrence indicates a genetic milieu with autosomal dominant pattern. Here, we present a case report of a young woman suffering from pelvic pain due to osteopoikilosis (OPK). The same disorder was later found in her son and daughter.

Sclerosing stromal tumor of the ovary associated with endometrial adenocarcinoma: A case report

1988 ◽  
Vol 29 (3) ◽  
pp. 392-398 ◽  
Author(s):  
Yasuhiro Katsube ◽  
Yasuhisa Iwaoki ◽  
Steven G. Silverberg ◽  
Atsushi Fujiwara
Keyword(s):  
Case Report ◽  
Endometrial Adenocarcinoma ◽  
Stromal Tumor ◽  
Sclerosing Stromal Tumor

scholarly journals A rare case of sclerosing stromal tumor of ovary with Meigs syndrome presenting with torsion

2014 ◽  
Vol 5 (4) ◽  
pp. 116-118
Author(s):  
Ketaki K Junnare ◽  
Pramod Tajne ◽  
Pushpalata R Naphade
Keyword(s):  
Rare Case ◽  
Frozen Section ◽  
Stromal Tumor ◽  
Ca 125 ◽  
Normal Ovary ◽  
Ovarian Mass ◽  
Medical Sciences ◽  
Sclerosing Stromal Tumor

A young primi para presented with a large solid ovarian mass with ascites and hydrothorax. She had raised CA 125 levels. She developed torsion of the mass after admission. At laparotomy the tumor was subjected to frozen section. The tumor was benign sclerosing stromal tumor of ovary. Uterus and normal ovary could be conserved. DOI: http://dx.doi.org/10.3126/ajms.v5i4.9518 Asian Journal of Medical Sciences 2014 Vol.5(4); 116-118

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