源自妇科疾病的腹膜假性粘液瘤:一个偶然的病理诊断

M. Samaila, A. Koledade, Rimamskep Ifusumu, S. Abdullahi, Usman Bappa, A. Adesiyun, F. Bakari, A. Makarfi, Ibrahim Adekanbi, Abbas Iliyasu, Sakina Ghazali
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摘要

腹膜假性黏液瘤是一种罕见的疾病,其特征是在骨盆和腹腔中存在和积聚凝胶状物质。这是一种不寻常的粘液性腹水的表现,其起源有争议,但通常与阑尾的原发性肿瘤有关。腹膜假性粘液瘤的诊断往往是偶然的探查剖腹手术,因为没有具体的诊断临床症状。我们报告三名女性妇科疾病偶然发现假性黏液瘤腹膜在没有阑尾或胃肠道肿瘤。组织活检用10%福尔马林固定,石蜡处理。代表性切片采用苏木精和伊红、周期性酸希夫、淀粉酶和粘卡明染色。女性3例,年龄25岁、42岁、50岁,分别有1年、5年、12年的腹胀、腹部肿块病史。老年女性还主诉阴道突出,体重明显下降。两名年轻女性临床诊断为晚期卵巢癌,而老年女性诊断为子宫阴道三度脱垂。三例患者均行剖腹探查,发现单侧左侧卵巢多分叶肿物,伴广泛的黏液性腹膜和网膜沉积。消化道未见明显病变,阑尾未见明显病理变化。其中2例患者行卵巢切除术并清除腹膜和网膜粘液物质,而第三例患者行阴道子宫切除术并清除腹膜胶质沉积物。胶状物质呈乳头状和多室囊性肿块,含有胶状液体。组织病理学诊断为假性黏液性腹膜瘤,背景为卵巢粘液性囊腺瘤,子宫阴道脱垂伴宫颈上皮表皮化。腹膜假性粘液瘤发生在没有原发性阑尾疾病的情况下,没有特定的诊断性临床症状。明确的诊断需要组织病理学分析,然而,当在没有大体病理的情况下出现粘蛋白池时,临床医生应该在剖腹手术中抱有高度的怀疑,特别是在患有良性妇科疾病的女性中。我们的病例在组织学上被划分为良性弥散性腹膜腺瘤病型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pseudomyxoma peritonei originating from gynecological diseases: An incidental pathological diagnosis
Psuedomyxoma peritonei is an uncommon disease characterized by the presence and accumulation of gelatinous material in the pelvis and abdominal cavity. It is an unusual manifestation of mucinous ascites of controversial origin, though often associated with a primary tumour of the appendix. Diagnosis of pseudomyxoma peritonei is often incidental during exploratory laparotomy because there are no specific diagnostic clinical symptoms. We report three females with gynaecological diseases with incidental finding of pseudomyxoma peritonei in the absence of appendiceal or gastrointestinal tumour. Tissue biopsies were fixed in 10% formalin and processed in paraffin wax. Representative sections were stained with haematoxylin & eosin, periodic acid Schiff, diastase and mucicarmine. Three females aged 25years, 42years and 50years presented respectively with a year, 5years and 12years history of abdominal swelling and abdominal mass. The older female also complained of vaginal protrusion with significant weight loss. Clinical diagnosis in the two younger females was advanced ovarian carcinoma, while the older female was diagnosed with third degree utero vaginal prolapse. All three had exploratory laparotomy which revealed unilateral multi lobulated left ovarian masses, with extensive mucinous peritoneal and omental deposits. There were no obvious gastrointestinal lesions and the appendices had no gross pathology. Two of the patients had oophorectomy with peritoneal and omental clearance of mucinous materials while the third patient had vaginal hysterectomy and peritoneal clearance of gelatinous deposits. The gelatinous materials showed papillary and multi locular cystic masses containing gelatinous fluid. Histopathological diagnosis of pseudomyxoma peritonei in a background of mucinous ovarian cystadenoma, and utero vaginal prolapse with epidermialization of the cervical lining epithelium was made. Pseudomyxoma peritonei occurs in the absence of a primary appendiceal disease and there are no specific diagnostic clinical symptoms. Definitive diagnosis requires histopathological analysis however, clinicians should entertain a high index of suspicion during laparotomy when mucin pools are present in the absence of gross pathology particularly in females with benign gynaecological diseases. Our cases were classed histologically into the benign disseminated peritoneal adenomucinosis type.
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