Gyneocology
Jila Agah; fatemeh borzoee; Narjes Heshmatifar
Volume 28, Issue 4 , September and October 2021, , Pages 502-508
Abstract
Introduction: Ovarian dermoid cysts are congenital developmental abnormalities, a dominant somatic cell layer. Dermoid cysts are formed more than the epidermis and skin attachments and are located in abnormal places. In this study, a female was introduced with a dermal ovarian cyst containing three adult ...
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Introduction: Ovarian dermoid cysts are congenital developmental abnormalities, a dominant somatic cell layer. Dermoid cysts are formed more than the epidermis and skin attachments and are located in abnormal places. In this study, a female was introduced with a dermal ovarian cyst containing three adult teeth. The patient has referred to the Sabzevar Vasei Hospital.
Case Report: A 35-year-old woman with nausea, suprapubic pain, abnormal vaginal bleeding refered to Vasaie Hospital Sabzevar, according to ultrasound and Diagnosis of left ovarian dermoid cyst, Laparoscopy was performed and the cyst was removed. The removed cysts contained mucous fluid, fatty substances, hair, and three teeth in particular. On abdominal examination, reported pain and tenderness in the left quadrant. Other clinical and rectal examinations was normal and at the cytology tests, the level of plasma hemoglobin and hematocrit was decreased.
Conclusion: According to the reported case, the cysts should be examined for genetic material, or stem cells.
Samaneh Bromand Novghabi; Seyyed Majid Ghazanfari; Azamsadat Hoseini Hoshyar; Maliheh Hasanzadehmofrad
Volume 19, Issue 3 , September and October 2012, , Pages 304-309
Abstract
Background: The association of an ovarian tumor with Ollier’s disease (multiple encondromatosis) is a known entity but chondrosarcoma and ovarian tumors is rare. Only one case with Ollier’s disease was reported. In this clinical presentation we report a patient with granulosa cell tumor and chondrosarcoma ...
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Background: The association of an ovarian tumor with Ollier’s disease (multiple encondromatosis) is a known entity but chondrosarcoma and ovarian tumors is rare. Only one case with Ollier’s disease was reported. In this clinical presentation we report a patient with granulosa cell tumor and chondrosarcoma Case Report: Our patient was a 20 year old woman with acute abdominal symptoms and adnexal mass. She had emergency surgery. Ovarian mass was removed and sent for pathologic study. Ovarian granulosa cell tumor was reported. In the next follow-up CTscan reported osteolitic mass of iliac bone. Biopsy was done and was compatible with chondrosarcoma of iliac. Then radical surgery and resection of iliac bon was performed. Due to the demand for fertility preservation, she was undergoing chemotherapy. Conclusion: There is a risk of malignant change to chondrosarcoma or other bone tumours in Ollier's Disease. The attractive point of this patient is the association of ovarian tumor with primary iliac chondrosarcoma that has not been reported .Concurrent findings may help future research in finding the cause, early diagnosis and appropriate treatment of tumors.