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Primary actinomycosis of the thigh – a rare soft tissue infection with review of literature

机译:大腿原发性放线菌病–一种罕见的软组织感染,已有文献复习

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Primary actinomycosis is a rare soft tissue infection which requires a high degree of clinical suspicion to diagnose and it should be differentiated from other chronic conditions like tuberculosis.DECLARATIONSCompeting interestsNone declaredFundingNo funding obtainedEthical approvalWritten informed consent was obtained from the patient or next of kinGuarantorRohan KhandelwalContributiorshipRK, PCM: Operating surgeons and involved in manuscript preparation. IJ: Pathologist; reported the histopathology slides SP, AS, SY: Assisting surgeons and helped in manuscript preparation PS, SS: Helped in review of literature and management of the patientReviewerJody ParkerCase report Section:A 42-year-old lady presented to the surgical OPD with complaints of a swelling with multiple discharging sinuses over her right thigh for the past two years. The swelling was insidious in onset and was gradually increasing in size. There was no history of any trauma or insect bite at the site of the lesion. The patient had no past history suggestive of tuberculosis or diabetes mellitus. She was postmenopausal for the last four years and had no past history of intrauterine contraceptive device insertion. She had been treated by multiple doctors in various centres, over the last 6 months and had taken extended courses of oral antimicrobial therapy.On examination there was a 15 cm x 20 cm, irregularly shaped, indurated swelling in the medial aspect of the right thigh extending from the perineum to mid-thigh (Figure 1). There were multiple sinuses draining yellow coloured pus along with sulphur granules. There were no other lesions elsewhere on the body.DownloadOpen in new tabDownload in PowerPointFigure 1 Actinomycotic lesion over the thigh extending to the perineum. Multiple openings of sinuses can be seenThe pus from the discharging sinuses was sent for microscopy and a biopsy from the lesion was sent for histopathological examination. Gram staining revealed Gram positive bacilli, but no organisms could be cultured. Histopathological examination confirmed the diagnosis of actinomycosis (Figure 2).DownloadOpen in new tabDownload in PowerPointFigure 2 High power view (100X) showing an actinomycotic colony in a background of chronic inflammationA MRI scan was done and it revealed multiple sinuses in the medial aspect of the right thigh extending to the underlying muscles (Figure 3). There were no lesions in the underlying bone.DownloadOpen in new tabDownload in PowerPointFigure 3 MRI image showing multiple sinuses extending till the underlying muscles. The bone appears to be normalThe patient was started on co-trimaxozole and cindamycin for a period of 1 month, after which the patient was taken up for surgical excision of the lesion followed by split skin grafting to cover the created defect (Figure 4). During excision, the whole lesion along with the involved muscle was removed. Multiple sinus tracks were encountered during surgery.DownloadOpen in new tabDownload in PowerPointFigure 4 Postoperative picture after resection of the lesion and split skin thickness graft in placeThe patient had a wound infection in the postoperative period, which responded to parental antibiotics. The patient was discharged on oral co-trimaxazole and clindamycin for 15 days following which only co-trimaxozole was continued for 2 months.The patient has been in regular follow-up and there has been no recurrence till after 1 year of surgery (Figure 5).DownloadOpen in new tabDownload in PowerPointFigure 5 Picture after one year of surgery, showing no signs of recurrence and a well healed scarDiscussion Section:Actinomycosis is subacute to chronic, suppurative granulomatous disease that tends to produce draining sinus tracts. This usually manifests as cervico-facial, thoracic or abdominal actinomycosis. It is most commonly caused by Actinomyces israelii in humans and Actinomycosis viscosus, Actinomycosis bovis, Actinomycosis naeslundii in animals. Actinomycosis is an anaerobic, gra
机译:原发性放线菌病是一种罕见的软组织感染,需要高度的临床怀疑才能诊断,应与其他慢性病(如结核病)区分开。竞争利益未宣布资金未获得资金伦理批准未从患者或近亲家中获得书面知情同意书担保人罗汉·坎德尔瓦尔沃尔(Rohan Khandelwal)供稿:外科医师,从事手稿的准备。 IJ:病理学家;报告组织病理学幻灯片SP,AS,SY:协助外科医生并协助手稿准备PS,SS:帮助复习患者的文献资料和治疗方法评论者乔迪·帕克病例报告部分:一名42岁的女士因手术原因向手术OPD提出投诉在过去的两年中,她的右大腿出现多个鼻窦肿胀。肿胀起病隐匿,大小逐渐增加。病变部位无任何外伤或昆虫叮咬的病史。该患者没有既往结核病或糖尿病的病史。她在绝经后的最后四年中,没有子宫内避孕器插入的历史。在过去的六个月中,她曾在多个中心接受过多位医生的治疗,并接受了长期的口服抗菌药物治疗。检查时,右大腿内侧出现15厘米x 20厘米,形状不规则,硬结肿胀从会阴延伸到大腿中部(图1)。有多个鼻窦排出黄色脓液和硫磺颗粒。身体其他部位没有其他病变。下载在新标签中打开在PowerPoint中下载图1大腿上放线放线菌病的病变延伸到会阴。可以看到鼻窦的多个开口将排出鼻窦的脓液送去进行显微镜检查,并从病变处进行活检以进行组织病理学检查。革兰氏染色显示革兰氏阳性菌,但无法培养任何生物。组织病理学检查证实了放线菌病的诊断(图2)。下载在新标签中打开在PowerPoint图2高倍率视图(100X)显示在慢性炎症背景下的放线菌菌落菌落进行了MRI扫描并显示了在内侧的多个窦右大腿延伸至基础肌肉(图3)。图3 MRI图像显示多个窦延伸到下层肌肉。骨骼似乎正常该患者开始接受三曲唑和cindamycin的治疗,持续了1个月,之后开始对该患者进行手术切除病灶,然后进行皮下移植以覆盖所产生的缺损(图4)。在切除过程中,整个病变以及所累及的肌肉都被去除了。手术过程中遇到多个窦道。患者口服co-trimaxazole和clindamycin出院15天,之后仅继续co-trimaxozole疗程2个月,患者进行了定期随访,直到手术1年后才复发。(图5图5手术一年后的图片,未见复发迹象且疤痕愈合良好讨论部分:放线菌病是慢性化脓性肉芽肿性疾病的亚急性病,容易产生引流性窦道。这通常表现为宫颈面部,胸部或腹部放线菌病。它最常见是由人类的以色列放线菌和粘性放线菌,牛放线菌,纳氏放线菌引起的。放线菌病是厌氧的

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