Retroperitoneal Pheochromocytoma: A Rare Tumour Presenting as Ovarian Mass

B. Dhananjaya, B. Thanmaye, G. Sowmya, M. Naveen
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Abstract

A 40 year old patient suffering from vague pain in the abdomen since 1 month, came with CT scan of abdomen and pelvis showing large lobulated cystic lesion of 11 x 10.6 x 9.7cms suggesting ? Left ovarian neoplasm. On exploratory laparotomy uterus and ovaries were normal and a mass of 10 x 9 cm was seen arising from the pelvis. The Histopathological report stated pheochromocytoma. The extra adrenal pheochromocytomas are rare tumors that originate from the chromaffin tissue of sympathetic nervous system.
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腹膜后嗜铬细胞瘤:以卵巢肿块表现的罕见肿瘤
患者40岁,腹部隐隐约约疼痛1个月,腹部及骨盆CT显示大分叶状囊性病变,11 × 10.6 × 9.7cm,提示?左卵巢肿瘤。剖腹探查时,子宫和卵巢正常,骨盆处可见一个10 × 9厘米的肿块。组织病理学报告为嗜铬细胞瘤。肾上腺外嗜铬细胞瘤是一种罕见的肿瘤,起源于交感神经系统的嗜铬组织。
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