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表现为盆腔恶性肿块的盆腔放线菌病:一例报告

Pelvic actinomycosis presenting as a malignant pelvic mass: a case report.

作者信息

Simsek Arife, Perek Asiye, Cakcak Ibrahim Ethem, Durgun Ali Vedat

机构信息

Istanbul University, Cerrahpasa School of Medicine, Department of General Surgery, 34098, Fatih, Istanbul, Turkey.

出版信息

J Med Case Rep. 2011 Jan 27;5:40. doi: 10.1186/1752-1947-5-40.

Abstract

INTRODUCTION

Pelvic actinomycosis constitutes 3% of all human actinomycosis infections. It is usually insidious, and is often mistaken for other conditions such as diverticulitis, abscesses, inflammatory bowel disease and malignant tumors, presenting a diagnostic challenge pre-operatively; it is identified post-operatively in most cases. Here we present a case that presented as pelvic malignancy and was diagnosed as pelvic actinomycosis post-operatively.

CASE PRESENTATION

A 48-year-old Caucasian Turkish woman presented to our clinic with a three-month history of abdominal pain, weight loss and difficulty in defecation. She had used an intra-uterine device for 16 years, however it had recently been removed. The rectosigmoidoscopy revealed narrowing of the lumen at 12 cm due to a mass lesion either in the wall or due to an extrinsic lesion that prevented the passage of the endoscope. On examination, there was no gynecological pathology. Magnetic resonance imaging showed a mass, measuring 5.5 × 4 cm attached to the rectum posterior to the uterus. The ureter on that side was dilated. Surgically there was a pelvic mass adhered to the rectum and uterine adnexes, measuring 10 × 12 cm. It originated from uterine adnexes, particularly ones from the left side and formed a conglomerated mass with the uterus and nearby organs; the left ureter was also dilated due to the pelvic mass. Because of concomitant tubal abscess formation and difficulty in dissection planes, total abdominal hysterectomy and bilateral salphingo-oophorectomy was performed (our patient was 48 years old and had completed her childbearing period). The cytology revealed inflammatory cells with aggregates of Actinomyces. Penicillin therapy was given for six months without any complication.

CONCLUSIONS

Pelvic actinomycosis should always be considered in patients with a pelvic mass especially in ones using intra-uterine devices, and who have a history of appendectomy, tonsillectomy or dental infection. Surgeons should be aware of this infection in order to avoid excessive surgical procedures.

摘要

引言

盆腔放线菌病占所有人类放线菌感染的3%。它通常隐匿起病,常被误诊为憩室炎、脓肿、炎症性肠病和恶性肿瘤等其他疾病,术前诊断具有挑战性;大多数病例是在术后确诊的。在此,我们报告一例表现为盆腔恶性肿瘤且术后被诊断为盆腔放线菌病的病例。

病例介绍

一名48岁的高加索土耳其女性因腹痛、体重减轻和排便困难3个月前来我院就诊。她使用宫内节育器16年,但最近已取出。直肠乙状结肠镜检查显示,由于壁内肿块或外部病变导致肠腔在12 cm处狭窄,妨碍了内镜通过。检查时,未发现妇科病理情况。磁共振成像显示一个5.5×4 cm的肿块附着于子宫后方的直肠。该侧输尿管扩张。手术中发现一个盆腔肿块附着于直肠和子宫附件,大小为10×12 cm。它起源于子宫附件,特别是左侧,并与子宫及附近器官形成一个融合性肿块;盆腔肿块还导致左侧输尿管扩张。由于合并输卵管脓肿形成且解剖层面困难,遂行全腹子宫切除术和双侧输卵管卵巢切除术(患者48岁,已完成生育)。细胞学检查发现炎性细胞及放线菌聚集。给予青霉素治疗6个月,无任何并发症。

结论

对于有盆腔肿块的患者,尤其是使用宫内节育器、有阑尾切除术、扁桃体切除术或牙科感染史的患者,应始终考虑盆腔放线菌病。外科医生应了解这种感染,以避免过度的手术操作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a617/3039605/2fb1ee2dcc3e/1752-1947-5-40-1.jpg

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