Department of Pathology and Laboratory Medicine, King Fahad Specialist Hospital, Omar Bin Thabet Street, Dammam 31444, Saudi Arabia.
Int J Gynecol Pathol. 2013 May;32(3):277-82. doi: 10.1097/PGP.0b013e31825f7c25.
We present a 27-yr-old female with gonadal dysgenesis (46, XY), who presented to our hospital with poor consciousness, aphasia, restlessness, and visual hallucination. Physical examination revealed normal breast development and normal external female genetalia. Computed tomography scan of the head and neck revealed the presence of brain edema, hydrocephalous, and a localized hypodense lesion in the hypothalamus. Her serum was positive for the anti-Ma2, which is associated with paraneoplastic encephalitis syndrome. Computed tomography of the abdomen revealed the presence of a 7.5×5.3×3.0 cm solid pelvic mass. Interestingly, a single microscopic focus of dysgerminoma was identified in a background of stromal fibrosis and focal dystrophic calcifications. No ovarian stroma or testicular tissue was identified. To our knowledge, this is the first case of gonadal dysgenesis presenting with anti-Ma2 paraneoplastic encephalitis with dysgerminoma. A discussion about paraneoplastic encephalitis with a microscopic dysgerminoma associated with anti-Ma2 antibody is presented.
我们报告了一例 27 岁的女性患者,患有性腺发育不全(46,XY),因意识不清、言语障碍、躁动不安和幻视而就诊于我院。体格检查发现乳房发育正常,外阴正常。头颅颈部 CT 扫描显示脑水肿、脑积水和下丘脑局灶性低密度病变。她的血清抗 Ma2 阳性,与副肿瘤性脑炎综合征相关。腹部 CT 显示有一个 7.5×5.3×3.0 cm 的盆腔实性肿块。有趣的是,在间质纤维化和局灶性营养不良性钙化的背景下,仅发现单个生殖细胞瘤的微观焦点。未发现卵巢间质或睾丸组织。据我们所知,这是首例性腺发育不全伴抗 Ma2 副肿瘤性脑炎伴生殖细胞瘤的病例。本文讨论了与抗 Ma2 抗体相关的伴微小生殖细胞瘤的副肿瘤性脑炎。