Yang Bin, Valluru Bimbadhar, Guo Ya-Ru, Cui Chunmao, Zhang Ping, Duan Wenshuai
Department of Radiology Department of Pulmonology, the First Affiliated Hospital of Dali University, Dali, People's Republic of China.
Medicine (Baltimore). 2017 Dec;96(52):e9040. doi: 10.1097/MD.0000000000009040.
Accessory spleen (Heterotopic/Ectopic) or splenunculus has been attributed to the failure of the fusion of splenic primordial buds-derived from dorsal mesentery (mesodermal mesenchymal in origin) during the 5th week of embryonic organogenesis or to an extreme degree of splenic lobulation with pinching off of the spleen tissue. The most common locations for accessory spleens are the hilum of the spleen followed by adjacent to the tail of the pancreas. The patients usually present with no clinical symptoms.
A 49-year-old female undergoing a routine medical examination- Abdominal Ultrasound revealed a pancreatic mass. She was admitted into the hospital for 3 days and was put under observation. There are no specific findings during the physical examination or any related abnormalities in the laboratory investigations.
Heterotopic spleen-an intrapancreatic accessory spleen (IPAS).
Noncontrast CT of the abdomen demonstrated a soft tissue mass with a clear boundary in the tail of the pancreas. On contrast examination-the arterial phase, it was markedly enhanced, homogenous congruity similar to that of spleen; on magnetic resonance imaging (MRI)-T2WI with fat suppressed sequence, it demonstrated a regular round clear edged mass in the pancreatic tail. On Diffusion Weighted Imaging (DWI), a mass with a clear boundary was observed within the parenchyma of the pancreatic tail. The mass showed a high signal on noncontrast MRI, while on contrast examination, the mass showed a strengthening signal with homogenous enhancement as that of spleen.
Heterotopic spleen presentation is a very rare asymptomatic clinical condition. During the routine medical examination - it presents mostly as a solitary benign round or oval mass with a clear boundary or as an ectopic focus, either in the pancreatic tail or adjacent to the pancreatic appendage, as an incidental finding. On Contrast CT, it shows as a homogeneously enhanced density- a strengthening mass lesion, in the pancreatic tail, similar to that of spleen.
Our case emphasizes the importance of recognizing IPAS radiological characteristics and typical variations in its presentation in an asymptomatic patient that could help the personnel to differentiate it from other mass lesions. Thus, recognizing imaging findings on Plain CT, Contrast CT and MRI plays a key role to form a conclusive diagnosis of an accessory spleen, which has to be clinically associated. So, surgeons should consider IPAS as a differential for which unnecessary resection and an unintended surgical procedure can be avoided.
副脾(异位/迷走)或脾小结被认为是由于胚胎器官发生第5周时,源自背侧肠系膜(起源于中胚层间充质)的脾原基芽融合失败,或由于脾叶极度分叶导致脾组织被挤压分离所致。副脾最常见的位置是脾门,其次是胰腺尾部附近。患者通常无临床症状。
一名49岁女性在进行常规体检——腹部超声检查时发现胰腺肿物。她入院观察3天。体格检查无特殊发现,实验室检查也无任何相关异常。
异位脾——胰腺内副脾(IPAS)。
腹部平扫CT显示胰腺尾部有一边界清晰的软组织肿块。增强检查——动脉期,肿块明显强化,均匀一致,与脾脏相似;在磁共振成像(MRI)——脂肪抑制T2WI序列上,胰腺尾部可见一规则圆形、边界清晰的肿块。在扩散加权成像(DWI)上,胰腺尾部实质内可见一边界清晰的肿块。该肿块在平扫MRI上呈高信号,增强检查时,肿块呈强化信号,强化均匀,与脾脏相同。
异位脾表现为一种非常罕见的无症状临床情况。在常规体检中——大多表现为单个边界清晰的良性圆形或椭圆形肿块,或为异位病灶,位于胰腺尾部或胰腺附件附近,为偶然发现。在增强CT上,表现为胰腺尾部密度均匀强化——强化的肿块病变,与脾脏相似。
我们的病例强调了识别IPAS放射学特征及其在无症状患者中典型表现变化的重要性,这有助于工作人员将其与其他肿块病变区分开来。因此,识别平扫CT、增强CT和MRI上的影像学表现对于形成副脾的确切诊断起着关键作用,且必须结合临床。所以,外科医生应将IPAS作为一种鉴别诊断,以避免不必要的切除和意外的手术操作。