Kodaganur Srinivas, Hosamani Ishwar R, Doddamani Muralidhar, Udaykumar K V
Department of General Surgery, KIMS, Hubli, Karnataka India.
Indian J Surg. 2016 Feb;78(1):54-6. doi: 10.1007/s12262-015-1344-2. Epub 2015 Sep 15.
Clinical diagnosis of abdominal masses remains a challenge to this day; in spite of the availability of advanced imaging facilities, we fail to reach a definitive diagnosis in a few cases and have to resort to a laparotomy, which reveals unexpected findings. We present a case of a 70-year-old lady who presented with pain abdomen and loss of appetite for 3 months; clinical examination revealed a fixed intra-abdominal firm to hard mass in the left iliac fossa. CT scan of the abdomen showed a large cystic hypodense lesion in the left iliac, lumbar and hypogastric region with no definite organ of origin. The patient underwent an exploratory laparotomy and in toto excision of the cyst; on opening the cyst wall, we found multiple daughter cysts in a pool of thick, purulent fluid. Microscopic examination confirmed the presence of a hydatid cyst Primary peritoneal hydatid cysts are a rare entity and constitute around 2 % of hydatid cysts found in the human body. Very few cases of primary peritoneal hydatid cyst have been reported from non-endemic areas, and this case report highlights the need to maintain a high index of suspicion while evaluating cystic abdominal swellings.
时至今日,腹部肿块的临床诊断仍是一项挑战;尽管有先进的影像检查设备,但仍有少数病例无法明确诊断,不得不进行剖腹探查,而探查结果往往出人意料。我们报告一例70岁女性患者,因腹痛和食欲不振3个月就诊;临床检查发现左髂窝有一固定的腹内实性至硬肿块。腹部CT扫描显示左髂窝、腰部和下腹部有一个大的囊性低密度病变,无法明确起源器官。患者接受了剖腹探查并完整切除囊肿;打开囊肿壁时,我们在浓稠的脓性液体中发现了多个子囊。显微镜检查证实为包虫囊肿。原发性腹膜包虫囊肿是一种罕见的疾病,约占人体包虫囊肿的2%。非流行地区报道的原发性腹膜包虫囊肿病例极少,本病例报告强调在评估腹部囊性肿物时需保持高度警惕。