Buehner M, Baker M S
Department of Obstetrics and Gynecology, Kaiser Permanente Medical Center, San Rafael, California.
Surg Gynecol Obstet. 1992 Oct;175(4):373-87.
Wandering spleen is an unusual entity, occurring in both sexes and at any age, but is more frequent in women of reproductive age and in children. Wandering spleen is probably most often a result of congenital anomalies of development of the dorsal mesogastrium, but acquired factors may have a role in certain instances. Patients present most commonly with an asymptomatic mass, mass and subacute abdominal or gastrointestinal complaints or with acute abdominal findings. Clinical diagnosis can be difficult, but noninvasive imaging procedures, such as sonography, nuclear scintigraphy, computed tomography and magnetic resonance imaging are usually diagnostic. Laboratory tests are usually nonspecific, but may occasionally reveal evidence of hypersplenism or functional splenia. Symptoms may remain limited or absent for long periods of time, but complications related to torsion or compression of abdominal organs by the spleen or the pedicle are quite common. Splenomegaly is usually a result of torsion of the pedicle and splenic sequestration. Significant morbidity and mortality rates seem to be considerably less than described in 1933 and limited primarily to patients presenting initially with acute abdominal findings. Management recommendations have varied, but recognition of a significant risk of postsplenectomy sepsis supports a conservative approach. Patients with limited symptomatology may be medically managed until they exhibit worsening symptoms indicating progressive splenic torsion or gastrointestinal compression. Detorsion and splenopexy may be considered a reasonable surgical option even in patients presenting with acute abdomen, if there is no evidence of infarction, thrombosis or hypersplenism. Splenic preservation is especially recommended in extremely young patients who are at particular risk for postsplenectomy sepsis. However, it should be noted that follow-up evaluation data on splenopexy patients are notably lacking. Splenectomy is ideally reserved for patients presenting with acute abdomen and splenic infarction or thrombosis or with hypersplenism and patients in whom splenopexy is technically unfeasible. Subtotal splenectomy and splenic autotransplantation may be of limited value. Pneumococcal, Hemophilus and meningococcal vaccines are indicated before elective splenectomy and shortly after nonelective splenectomy. Antibiotic prophylaxis is recommended for those at particular risk. Prospective studies are unlikely, but extended follow-up information on patients already reported, particularly those managed expectantly or with conservative surgical measures, is needed.
游走脾是一种罕见的病症,可发生于任何年龄和性别,但在育龄期女性和儿童中更为常见。游走脾很可能大多是由于胃背系膜先天性发育异常所致,但在某些情况下后天因素也可能起作用。患者最常见的表现是无症状肿块、肿块伴亚急性腹部或胃肠道不适,或出现急性腹部症状。临床诊断可能困难,但超声、核素扫描、计算机断层扫描和磁共振成像等非侵入性成像检查通常可作出诊断。实验室检查通常无特异性,但偶尔可能显示脾功能亢进或功能性脾的证据。症状可能长期局限或无症状,但与脾脏或脾蒂扭转或压迫腹部器官相关的并发症相当常见。脾肿大通常是脾蒂扭转和脾内血液滞留的结果。与1933年所描述的情况相比,目前明显的发病率和死亡率似乎要低得多,且主要限于最初表现为急性腹部症状的患者。治疗建议各不相同,但认识到脾切除术后败血症的重大风险支持采取保守方法。症状有限的患者可进行药物治疗,直到症状恶化表明脾脏扭转或胃肠道受压进展。即使是表现为急腹症的患者,如果没有梗死、血栓形成或脾功能亢进的证据,扭转复位和脾固定术也可被视为一种合理的手术选择。对于有脾切除术后败血症特别风险的极年轻患者,尤其建议保留脾脏。然而,应当指出,关于脾固定术患者的随访评估数据明显缺乏。脾切除术理想情况下适用于表现为急腹症和脾梗死或血栓形成的患者、脾功能亢进的患者以及脾固定术在技术上不可行的患者。次全脾切除术和脾自体移植术的价值可能有限。在择期脾切除术前以及非择期脾切除术后不久,应接种肺炎球菌、嗜血杆菌和脑膜炎球菌疫苗。对于有特别风险的患者,建议预防性使用抗生素。前瞻性研究不太可能进行,但需要对已报告患者进行长期随访信息,尤其是那些接受观察或保守手术治疗的患者。