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放线菌病所致乙状结肠假肿瘤:1例罕见病例

Sigmoid colon pseudotumor of actinomycosis: a rare case.

作者信息

Lesmana Andy, Wirdhani Vika, Perangin Angin Lenti B R, Muzakky Muhamad I, Hayon Stefi G V, Sholihah Mentari M, Hanif Muhammad I

机构信息

Surgery Department, Dr. Sitanala Central Hospital, Tangerang, Indonesia.

Internal Medicine Department, Dr. Sitanala Central Hospital, Tangerang, Indonesia.

出版信息

J Surg Case Rep. 2024 Jan 4;2024(1):rjad697. doi: 10.1093/jscr/rjad697. eCollection 2024 Jan.

Abstract

UNLABELLED

Actinomycosis is a chronic suppurative infection caused by gram-positive bacteria, Actinomyces, which commonly colonize the oral cavity, urogenital tract and gastrointestinal tract. It causes opportunistic infection where the mucosal barrier is compromised and is often misdiagnosed as malignancy. We report a case of a 58-year-old female with severe abdominal pain and a palpable tender mass in the left lower quadrant. Computed tomography scan with contrast showed thickening of the transverse, descending to sigmoid colon wall and intense contrast enhancement resembling colitis with mesenteritis. At laparotomy, we found an adherent mass involving sigmoid colon with adjacent small bowel and peritoneum. We decided to perform adhesiolysis and Hartmann procedure. The culture result was negative, whereas the biopsy of sigmoid colon revealed characteristic sulfur granules of actinomycosis colony. Intravenous antibiotic combination of ceftazidime and metronidazole was administered for 14 days followed by complete resolution of symptoms. Histopathological and bacteriological examinations are keys to diagnose actinomycosis. Patients require long-term antibiotic therapy, but surgery is often required because preoperative diagnosis is difficult.

MAIN NOVEL ASPECTS?: We presented the rare case of intra-abdominal actinomycosis in IndonesiaThe case was challenging to diagnose pre-operatively based on physical examination andExploratory laparotomy revealed pseudotumor mimicking advanced stage of colon neoplasm.

摘要

未标注

放线菌病是由革兰氏阳性菌放线菌引起的慢性化脓性感染,放线菌通常定植于口腔、泌尿生殖道和胃肠道。它会在黏膜屏障受损时引发机会性感染,且常被误诊为恶性肿瘤。我们报告一例58岁女性病例,该患者有严重腹痛,左下腹可触及压痛性肿块。增强计算机断层扫描显示横结肠、降结肠至乙状结肠壁增厚,强化明显,类似结肠炎合并小肠炎。剖腹探查时,我们发现一个粘连性肿块累及乙状结肠及相邻小肠和腹膜。我们决定进行粘连松解术和哈特曼手术。培养结果为阴性,而乙状结肠活检显示有放线菌病菌落特征性的硫磺颗粒。给予头孢他啶和甲硝唑静脉联合抗生素治疗14天,随后症状完全缓解。组织病理学和细菌学检查是诊断放线菌病的关键。患者需要长期抗生素治疗,但由于术前诊断困难,通常还需要手术治疗。

主要新特点?:我们报道了印度尼西亚罕见的腹内放线菌病病例。该病例术前基于体格检查诊断具有挑战性,剖腹探查发现假肿瘤,类似晚期结肠肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff2b/10766591/54672dd5ab30/rjad697f1.jpg

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