Aziz Hassan, Hao Michelle, Merchant Alam, Alfson Daniel, Foran Chris, Raashid Sheikh M
Department of Surgery, Division of Hepatobiliary Surgery, Keck School of Medicine, University of Southern California Medical Center, Los Angeles County, Los Angeles, CA, United States.
Department of Surgery, Division of Hepatobiliary Surgery, Keck School of Medicine, University of Southern California Medical Center, Los Angeles County, Los Angeles, CA, United States.
Int J Surg Case Rep. 2020;74:218-221. doi: 10.1016/j.ijscr.2020.08.047. Epub 2020 Aug 29.
Our case report describes a patient where multiple laparoscopies five years from initial presentation of symptoms were performed prior to laparotomy for benign multi-cystic peritoneal mesothelioma (BMPM), which has not been documented.
A 61-year-old woman presented with years of chronic abdominal pain. Computerized tomography (CT) demonstrated a multi-cystic mass near the porta hepatis, and ultrasound was concerning for contained gallbladder perforation. Fine needle aspiration (FNA) demonstrated benign ductal epithelial cells in a background of mucin and bile without the presence of malignant cells. During laparotomy, a cystic mass attached to the porta hepatis seen emanating from the small bowel mesentery, and additional small cystic lesions through the abdomen were removed. The specimen, measuring 26 × 18 × 8 cm, showed multi-loculated cysts filled with serous fluid.
BMPM is a rare neoplasm of mesothelioma cells originating from serosa of viscous organs. BMPMs appear as cystic structures with thin walls containing mucinous/gelatinous fluid. Microscopic features include a lack of invasion and no increased cellularity in the stroma, with or without inflammation (Myers & Babiker, 2018). It is postulated to be either a reactive or neoplastic process. There is no gold-standard treatment for BMPM. Our case is unique in the sense that our patient required several surgical biopsies before final diagnosis could be made.
This case highlights the difficulty of diagnosing BMPM and differentiating it from malignant diseases that can present similarly and can be associated with significantly worse prognosis. Defined management strategies have yet to be demonstrated.
我们的病例报告描述了一名患者,在因良性多囊性腹膜间皮瘤(BMPM)接受剖腹手术之前,在出现症状五年后进行了多次腹腔镜检查,这种情况此前未见文献记载。
一名61岁女性因多年慢性腹痛就诊。计算机断层扫描(CT)显示肝门附近有一个多囊性肿块,超声检查怀疑胆囊穿孔。细针穿刺抽吸(FNA)显示在黏液和胆汁背景中有良性导管上皮细胞,无恶性细胞。剖腹手术时,可见一个附着于肝门的囊性肿块,起源于小肠系膜,还切除了腹部其他小的囊性病变。标本大小为26×18×8厘米,显示为多个充满浆液的囊肿。
BMPM是一种罕见的间皮瘤细胞肿瘤,起源于内脏器官的浆膜。BMPM表现为薄壁的囊性结构,内含黏液样/胶冻样液体。显微镜下特征包括无浸润,间质细胞数量无增加,有或无炎症(迈尔斯和巴比克,2018年)。推测其为反应性或肿瘤性过程。BMPM尚无金标准治疗方法。我们的病例独特之处在于,患者在最终确诊前需要进行多次手术活检。
本病例突出了诊断BMPM的困难,以及将其与可能表现相似且预后明显更差的恶性疾病相鉴别的困难。尚未证明有明确有效的管理策略。