Shrestha Ashish Lal, Shrestha Pradita
Department of General Surgery, United Mission Hospital, Tansen, Palpa, Nepal.
Case Rep Gastrointest Med. 2017;2017:9896856. doi: 10.1155/2017/9896856. Epub 2017 Dec 25.
Splenic Pseudocyst (SP) is a diagnostic rarity, with cystic lesions of spleen themselves being uncommon. Establishing a preoperative diagnosis could help in specific management but this is rather challenging. Here we present a common presentation of an uncommon diagnosis.
A 47-year-old lady, previously well, presented to the outpatient clinic with intermittent left hypochondrial pain radiating towards left shoulder for 2 months not associated with fever, jaundice, or weight loss. Abdominal examination revealed nontender hepatosplenomegaly. The initial abdominal ultrasonogram (USG) was suggestive of a hydatid cyst, for which she received a course of antihelminthics. At follow-up, after finding no clinical improvement and radiological worsening, she underwent an exploratory laparotomy. A cyst replacing entire lower pole and a significant portion of splenic hilum was found. Total splenectomy was performed. The specimen was reported to be a SP.
SP is a unique entity, usually misdiagnosed as a parasitic lesion and often treated with antihelminthic medicines. The natural course of disease, however, follows a subsequent failure of symptom resolution and radiological worsening that ultimately demands surgical attention. Based on size, location, and intraoperative findings, either total or partial splenectomy is required. The final histopathological report often presents a diagnostic surprise.
脾假性囊肿(SP)是一种罕见的诊断,脾脏的囊性病变本身并不常见。术前做出诊断有助于进行针对性治疗,但这颇具挑战性。在此,我们呈现一个罕见诊断的常见病例。
一位47岁的女性,既往身体健康,因间歇性左季肋部疼痛并向左肩部放射2个月就诊于门诊,疼痛与发热、黄疸或体重减轻无关。腹部检查发现肝脾肿大但无压痛。最初的腹部超声检查(USG)提示为包虫囊肿,为此她接受了一个疗程的抗蠕虫治疗。在随访中,发现临床症状无改善且影像学表现恶化后,她接受了剖腹探查术。术中发现一个囊肿取代了整个脾下极及脾门的大部分。遂行全脾切除术。术后标本报告为脾假性囊肿。
脾假性囊肿是一种独特的疾病,通常被误诊为寄生虫性病变,且常使用抗蠕虫药物治疗。然而,疾病的自然病程随后会出现症状未缓解且影像学表现恶化的情况,最终需要手术治疗。根据囊肿大小、位置及术中所见,可能需要行全脾切除术或部分脾切除术。最终的组织病理学报告往往会带来诊断上的意外。