Bekheit Mohamed, Katri Khaled Mohamed, Ezzat Tarek
Alexandria Main University Hospital, Alexandria, Egypt.
Int J Surg Case Rep. 2012;3(5):151-4. doi: 10.1016/j.ijscr.2011.10.020. Epub 2012 Jan 20.
Several congenital anomalies of the spleen have been reported. The polysplenia is a rare anomaly in which the normal spleen is replaced with two or more smaller spleens. The wandering spleen is another anomaly resulting from the laxity of the splenic ligaments. The concomitance of both anomalies is very rare.
A 22-year old female patient presented with intermittent left hypochondrial pain for more than a year. After a thorough examination of the patient, she only had bilateral accessory nipples. Routine laboratory investigations were all normal. An abdominal ultrasound U/S scan was unremarkable except for a ptotic spleen. with a large splenule 5cm×3cm located near the fundus of the stomach. These findings were confirmed by a CT scan. A decision for a surgical intervention was then made, and the laparoscopic approach was chosen which revealed the condition. Laparoscopic removal of the wandering part was executed. The patient discharged on the first post-operative day.
The decision making in cases of wandering spleen is not always the same. The association of a wandering spleen with polysplenia is an asset to the surgical decision, along with the age of the patient.
The laparoscopic approach is an important tool in the diagnosis and management of wandering spleen. The diagnosis of polysplenic anomaly could provide a guidance for the surgical strategy in patients with wandering spleen.
已报道了几种脾脏先天性异常。多脾症是一种罕见的异常情况,正常脾脏被两个或更多个较小的脾脏所取代。游走脾是另一种由脾韧带松弛引起的异常。这两种异常同时存在非常罕见。
一名22岁女性患者出现间歇性左季肋部疼痛一年多。对该患者进行全面检查后,发现她仅有双侧副乳头。常规实验室检查均正常。腹部超声(U/S)扫描除脾脏下垂外无异常,在胃底附近有一个5cm×3cm的大副脾。CT扫描证实了这些发现。随后决定进行手术干预,并选择了腹腔镜手术方式,术中明确了病情。实施了腹腔镜下切除游走部分的手术。患者术后第一天出院。
游走脾病例的决策并不总是相同的。游走脾与多脾症的关联以及患者年龄对手术决策有帮助。
腹腔镜手术方式是游走脾诊断和治疗的重要工具。多脾异常的诊断可为游走脾患者的手术策略提供指导。