Mbarki C, Ben Abdelaziz A, Sahnoun R, El Kadhi Y, Douik F, Hsayaoui N, Mezghenni S, Oueslati H
Service de gynécologie obstétrique, hôpital de Ben Arous-Yesminette, Ben Arous, Tunisie.
Service de gynécologie obstétrique, hôpital de Ben Arous-Yesminette, Ben Arous, Tunisie.
Gynecol Obstet Fertil. 2016 Mar;44(3):168-74. doi: 10.1016/j.gyobfe.2016.01.003. Epub 2016 Feb 5.
Actinomycosis is a rare little known granulomatous suppurative disease, more common in women, aided by the use of contraceptive purposes intrauterine device (IUD). Pelvic location is the rarest with an extension to adjacent organs making preoperative diagnosis difficult and misleading clinical presentation. Early diagnosis of this affection determines the therapeutic strategy and avoids mutilating interventions especially in young women.
We reviewed the record of women who consulted the department of obstetrics and gynecology at Ben Arous hospital (Tunisia) between January 2003 and December 2013 for a pelvic pain syndrome and in whom diagnosis of actinomycosis was suspected by clinical and imaging and confirmed by pathology.
Eight cases of gynecologic abdominopelvic actinomycosis were diagnosed during the study period. Seven patients were carriers of an intrauterine device, with an average duration of 5 years wearing. Functional signs were essentially pelvic pain and fever. Physical examination of patients mainly showed two clinical presentations: a pelvic tumor syndrome or abdominopelvic and an array of pelvic abscess or pelvic inflammatory disease. Radiological investigations were allowed to suspect the diagnosis of actinomycosis only in one patient, in whom percutaneous biopsy confirmed the histological diagnosis without resorting to a surgical procedure. Operative procedures performed were varied as appropriate. The diagnosis of actinomycosis was made by pathology without any cases of bacterial isolation. All patients received antibiotic treatment with penicillin. The subsequent evolution was favorable.
The diagnosis of actinomycosis should be considered in any invasive abdominal mass of neoplastic appearance and in case of table of genital infection especially in patients bearing IUD for 5 years or more.
放线菌病是一种罕见的鲜为人知的肉芽肿性化脓性疾病,在女性中更为常见,宫内节育器(IUD)用于避孕目的会增加其发病几率。盆腔部位的放线菌病最为罕见,可蔓延至邻近器官,导致术前诊断困难且临床表现具有误导性。早期诊断这种疾病可确定治疗策略,并避免尤其是对年轻女性进行致残性干预。
我们回顾了2003年1月至2013年12月期间在突尼斯本阿鲁斯医院妇产科就诊的患有盆腔疼痛综合征的女性病历,这些女性经临床和影像学检查怀疑患有放线菌病,并经病理学确诊。
在研究期间诊断出8例妇科腹盆腔放线菌病。7例患者携带宫内节育器,平均佩戴时间为5年。功能症状主要为盆腔疼痛和发热。患者的体格检查主要表现为两种临床症状:盆腔肿瘤综合征或腹盆腔肿瘤综合征,以及一系列盆腔脓肿或盆腔炎。仅1例患者通过放射学检查怀疑患有放线菌病,经皮活检在未进行手术的情况下证实了组织学诊断。所进行的手术操作根据具体情况各不相同。放线菌病的诊断通过病理学做出,无细菌分离病例。所有患者均接受青霉素抗生素治疗。随后的病情发展良好。
对于任何具有肿瘤外观的侵袭性腹部肿块以及生殖器感染病例,尤其是佩戴宫内节育器5年及以上的患者,均应考虑放线菌病的诊断。