Abstract
Introduction
An epidermoid cyst in an intrapancreatic accessory spleen (ECIPAS) is a rare non-neoplastic cyst, typically occurring in the pancreatic tail. It is difficult to preoperatively differentiate ECIPAS from other types of pancreatic neoplastic cysts.
Case presentation
We herein report a case of a 32-year-old man with a cystic tumor in the tail of the pancreas. The patient underwent a laparoscopic spleen-preserving distal pancreatectomy, and histological examination revealed the presence of ECIPAS. In addition, we also performed a literature review of 42 case reports of ECIPAS.
Conclusion
Although the preoperative diagnosis of ECIPAS is relatively difficult, familiarity with the imaging features, the clinical presentation and the location of the cyst could lead to a correct preoperative diagnosis of ECIPAS, which might thereby reduce the number of unnecessary resections.
Keywords: epidermoid cyst, accessory spleen, pancreas
Introduction
An epidermoid cyst in an intrapancreatic accessory spleen (ECIPAS) is extremely rare, with the prevalence of 1.7% in general population.1 The differential diagnosis of pancreatic cystic lesions is often challenging because of their similar findings on imaging. It is difficult to preoperatively differentiate ECIPAS from the “other” cystic neoplasms, such as a pancreatic pseudocyst, serous cystic neoplasm, mucinous cystic neoplasm, intraductal papillary mucinous neoplasm and lymphoepithelial cyst, or a solid pancreatic tumor, such as a pancreatic neuroendocrine tumor and solid pseudopapillary tumor, by using conventional imaging. Of the 51 cases of ECIPAS that have been reported in the English literature, only 5 cases were correctly diagnosed based on preoperative imaging.2–43 As ECIPAS is a non-neoplastic pancreatic cyst and has no malignant potential, a correct preoperative diagnosis could thereby reduce the number of unnecessary surgical resections of the pancreas. Herein, we report a case of a 32-year-old male with an ECIPAS and make a comprehensive review of the literature.
Case presentation
A 32-year-old male was admitted to The First Affiliated Hospital with a mass lesion on the pancreatic tail that was detected by abdominal ultrasound during an annual health checkup. No history of trauma or pancreatitis was recorded. He had normal vital signs and abdominal examination. Initial laboratory data also showed no abnormalities, including those for tumor markers such as carcinoembryonic antigen (CEA) or carbohydrate antigen 19-9 (CA19-9). Abdominal computed tomography (CT) revealed a well-defined cystic neoplasm, which was located in the tail of pancreas and approaching to splenic hilum (Figure 1A), without enhancement in the arterial phase (Figure 1B) and the portal phase (Figure 1C). Additionally, endoscopic ultrasonography (EUS) showed a 3.5 cm multilocular cystic lesion in the pancreatic tail with an internal nodule (Figure 1D). The cystic tumor did not communicate with the main pancreatic duct.
Figure 1.
The abdominal computed tomography (CT) scan confirmed a well-defined cystic neoplasm in the pancreatic tail (A), without enhancement in the arterial phase (B) and the portal phase (C). Endoscopic ultrasonography (EUS) showed a 3.5 cm multilocular cystic lesion in the pancreatic tail with an internal nodule (D).
Upon diagnosis of mucinous cystic neoplasms, the patient underwent a laparoscopic spleen-preserving distal pancreatectomy. Macroscopic analysis revealed that the mass in the tail of the pancreas was 4 cm at its greatest diameter and consisted of parenchymal and cystic components (Figure 2A). The gross pathology showed a well-demarcated, multilocular mass, containing colorless serous fluid. Microscopic analysis revealed a multilocular cyst surrounded by accessory splenic tissue in the pancreas parenchyma, and the cyst wall showed a thin multilayered squamous epithelium (Figure 2B). The final pathological diagnosis was epidermoid cyst originating from an intrapancreatic accessory spleen. His postoperative course was uneventful and he was discharged 8 days after the surgery.
Figure 2.
(A) Gross appearance of the epidermoid cyst in an intrapancreatic accessory spleen (ECIPAS), with 4 cm at its greatest diameter. (B) Microscopic analysis revealed a multilocular cyst surrounded by accessory splenic tissue in the pancreas parenchyma, and the cyst wall showed a thin multilayered squamous epithelium (H&E staining, ×50).
Ethical approval
The study was approved by the ethics committee of The First Affiliated Hospital of Zhejiang University School of Medicine. Written informed consent was obtained from the patient to have the case details and any accompanying images published.
Discussion
Accessory spleens occur in ~10% of the population and can be found in various anatomic locations other than the splenic hilum. Approximately 20% of accessory spleens occur in or around the tail of the pancreas.1 Epidermoid cysts of the spleen are rare entities, comprising <10% of true non-parasitic splenic cysts.44 An ECIPAS is extremely rare, with only a few reports describing their clinical characteristics. Currently, with the advancement of imaging techniques, such as CT, magnetic resonance imaging (MRI) and EUS, an increasing number of ECIPASs have been detected.
Since Davidson et al2 reported the first case of ECIPAS in 1980, 41 articles and 50 patients have been reported in the English literature (Table 1). Including the present case, 20 cases were men and 32 cases were women. The mean age of the patients was 45.4 years (range 12–70 years), and 32 cases (61.5%) were younger than 50 years. Additionally, >50% of the cases were incidentally detected6,7,10,12,13,16,17,19–22,24–26,29–31,33,35,39,41–43 while the other symptoms included nausea, vomiting, abdominal pain and discomfort, back pain, epigastric pain and fever. In all cases, the tumors were located on the pancreatic tail. The cyst appeared to be multilocular in 31 cases and unilocular in 14 cases (no information for 7 cases). The average cyst size was 4.3 cm (range 1.4–15 cm). As ECIPAS occurs at a relatively young age and it is located in the pancreatic tail, it is always necessary to differentiate ECIPAS when identifying a pancreatic tail cystic mass in young patients.
Table 1.
Reported studies of an ECIPAS in the English language literature
| Case | Authors | Sex/age | Symptom | Location | Size (cm) | Cyst | CA19-9 | CT | MRI | Preoperative diagnosis | Surgery |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Davidson et al2 | M/40 | Nausea | Tail | 5.5 | Multilocular | NI | Cystic lesion surrounded by thin rim of tissue | NI | Pseudocyst, cystadenoma and cystadenocarcinoma | DP |
| 2 | Hanada et al3 | M/51 | Abdominal pain | Tail | 6 | NI | NI | Cystic mass with a rim of dense density | NI | Pseudocyst | DP |
| 3 | Morohoshi et al4 | F/32 | Abdominal pain | Tail | 6 | Unilocular | Normal | Well-demarcated cystic lesion | NI | Pancreatic cyst | Cyst removal |
| 4 | Nakae et al5 | F/37 | Epigastric pain | Tail | 6.5 | Unilocular | NI | Cystic lesion with a thin wall of high density | T1 low, T2 high | Pancreatic cyst | SPDP |
| 5 | Tang et al6 | M/38 | Asymptomatic | Tail | 1.4 | Multilocular | NI | Well-demarcated hypodense lesion | NI | NI | DP |
| 6 | Furukawa et al7 | M/45 | Asymptomatic | Tail | 2 | Multilocular | NI | Peripherally enhanced area, its density is equal to the spleen | NI | Primary cystic neoplasm | DP |
| 7 | Higaki et al8 | F/46 | Left back pain | Tail | 3 | Multilocular | + | Oval nodule with a distinct margin | NI | Malignant tumor | DP |
| 8 | Tateyama et al9 | F/67 | Abdominal pain | Tail | 3 | Multilocular | + | Cystic mass of low density | NI | NI | DP |
| 9 | Sasou et al10 | F/49 | Asymptomatic | Tail | 4.3 | Multilocular | NI | NI | NI | Pancreatic cystic tumor | DP |
| 10 | Choi et al11 | F/54 | Epigastric pain | Tail | 15 | Multilocular | NI | Major cystic component, small solid component with the same homogeneous attenuation as in the spleen | Cyst: T1 low, T2 high; solid lesion: T1 low, T2 intermediate-high | Benign cyst of the pancreas or accessory spleen | DP |
| 11 | Tsutsumi et al12 | M/51 | Asymptomatic | Tail | 2.5 | Multilocular | Normal | Well-demarcated cystic lesion containing a solid portion | Cystic lesion containing a solid portion | Benign cyst of the pancreas | DP |
| 12 | Horibe et al13 | M/48 | Asymptomatic | Tail | 2 | Unilocular | + | No substance in the cyst by enhanced image | NI | Mucin-producing pancreatic tumor | DP |
| 13 | Sonomura et al14 | F/45 | Epigastric pain | Tail | 3.5 | Multilocular | NI | Parenchymal medial lesion with calcification and cystic lateral lesion | NI | Cystadenocarcinoma or solid tumor of the pancreas | DP |
| 14 | Fink et al15 | F/12 | Fever | Tail | 10 | Multilocular | NI | Rim enhancing cystic lesion, with a medial mural nodule | NI | Infected abdominal cyst | Cyst removal |
| 15 | Yokomizo et al16 | M/38 | Asymptomatic | Tail | 3.0 | Multilocular | + | NI | Cyst: T2 super-high, cyst wall: delineated enhancement | MCN, adenocarcinoma and ECIPAS | DP |
| 16 | Kanazawa et al17 | F/58 | Asymptomatic | Tail | 2.5 | Multilocular | + | Septated low-density area | Cystic component: T1 hypo, T2 hyper | MCN | SPDP |
| 17 | Watanabe et al18 | F/55 | Postprandial epigastralgia | Tail | 3 | Multilocular | + | Multilocular cystic tumor. No protruded lesion in the inner lumen | T1 low, T2 high | Mucinous cystadenoma and cystadenocarcinoma | DP |
| 18 | Won et al19 | M/32 | Asymptomatic | Tail | 7.5 | Unilocular | + | Well-circumscribed cystic mass with inner fluid debris or hemorrhagic fluid | NI | Pancreatic pseudocyst | SPDP |
| 19 | Won et al19 | F/49 | Abdominal pain | Tail | 2.0 | Multilocular | Normal | Well-circumscribed cystic tumor with septation | NI | Serous or mucinous cystadenoma | Laparoscopic DP |
| 20 | Ru et al20 | M/41 | Asymptomatic | Tail | 2.5 | Unilocular | NI | Well-circumscribed tumor which partially compressed the spleen | NI | Cystic lesion of the pancreas | DP |
| 21 | Itano et al21 | M/40 | Asymptomatic | Tail | 4.0 | Unilocular | Normal | Solid component with the same homogeneous attenuation as the spleen | Cyst: T1/T2 high; solid component: T1 intermediate-low | ECIPAS | DP |
| 22 | Servais et al22 | F/52 | Asymptomatic | Tail | 11.5 | Multilocular | + | Cystic mass which was thin walled and contained single peripheral septation | NI | Malignant pancreatic neoplasm | DP |
| 23 | Gleeson et al23 | F/32 | Abdominal pain | Tail | 1.5 | Unilocular | NI | Demarcated cyst without septation, calcification and satellite lesions | NI | Pancreatic cystic neoplasm | DP |
| 24 | Zhang and Wang24 | F/26 | Asymptomatic | Tail | 2.5 | Unilocular | Normal | Cystic wall revealed a density similar to that of the pancreas | NI | Primary MCN | SPDP |
| 25 | Reiss et al25 | M/49 | Asymptomatic | Tail | 3.6 | Multilocular | NI | Heterogeneously enhancing mass | NI | MCN | DP |
| 26 | Kadota et al26 | F/57 | Asymptomatic | Tail | 6 | Multilocular | Normal | Cystic wall: a partial enhancement | NI | Pancreatic cystic tumor | DP |
| 27 | Kadota et al26 | F/70 | Asymptomatic | Tail | 1.7 | NI | + | Cystic mass lesion | NI | MCN | DP |
| 28 | Kadota et al26 | M/37 | Asymptomatic | Tail | 10 | NI | + | Cystic mass lesion with a partial enhancement of the cystic wall | NI | Serous cystic tumor or lymphoepithelial cyst | DP |
| 29 | Itano et al27 | M/67 | Epigastric pain | Tail | 1.5 | Unilocular | + | Cystic tissue and smooth solid component | Cyst: T1 intermediate, T2 high. Solid lesion: T1 intermediate-low | ECIPAS | Laparoscopic DP |
| 30 | Horn and Lele28 | M/62 | Abdominal pain | Tail | 4.8 | Multilocular | NI | Left-sided retroperitoneal mass with a possible cystic component | NI | NI | DP |
| 31 | Iwasaki et al29 | F/36 | Asymptomatic | Tail | 3.4 | Unilocular | + | Septate low-density lesion, with an area showing higher degree of enhancement than the pancreas | NI | MCN | Laparoscopic DP |
| 32 | Yamanishi et al30 | F/55 | Asymptomatic | Tail | 2.5 | Unilocular | + | Cyst wall was relatively thick, but not enhanced | Cyst: T1 slightly high, T2 strongly high | MCN | DP |
| 33 | Urakami et al31 | F/50 | Asymptomatic | Tail | 3.0 | Unilocular | NI | Single cyst with a contrasted mass beside it | Cyst: T1 low, T2 high | ECIPAS | Laparoscopic SPDP |
| 34 | Khashab et al32 | F/49 | Abdominal pain | Tail | 2.3 | Unilocular | NI | Solid mass | NI | PNET | Laparoscopic SPDP |
| 35 | Harris et al33 | F/39 | Asymptomatic | Tail | 2.5 | NI | NI | Stable hypodense lesion | Pancreatic cystic neoplasm | Malignant cystic tumor | Laparoscopic DP |
| 36 | Hong et al34 | F/54 | Abdominal discomfort | Tail | 2 | Multilocular | NI | Cystic mass | NI | NI | SPDP |
| 37 | Hamidian Jahromi et al35 | F/36 | Asymptomatic | Tail | 5 | Multilocular | NI | Cystic lesion | NI | NI | DP |
| 38 | Zavras et al36 | F/63 | Nausea and vomiting | Tail | 12.6 | NI | + | Mass lesion with solid and cystic components | NI | Malignant tumor of the pancreas | DP |
| 39 | Kumamoto et al37 | M/39 | Diarrhea | Tail | 3.8 | NI | + | A cyst lesion, surrounded by a crescent-like solid component with the same enhancement as the spleen | Typical findings of an intrapancreatic accessory spleen | ECIPAS | Laparoscopic SPDP |
| 40 | Kwak et al38 | F/21 | Abdominal pain and fever | Tail | 2.5 | Multilocular | Normal | The wall of the cyst was relatively regular, thick and enhanced | Cyst: T1 iso, T2 hyper. Rim showed hyperintensity in DWI | SPT | Laparoscopic DP |
| 41 | Kato et al39 | F/33 | Asymptomatic | Tail | 3 | Multilocular | Normal | The densities of the solid component and spleen on enhanced CT were similar | The intensity of the solid component on T1 and T2 was similar to that of the spleen | SPT and NET | Laparoscopic SPDP |
| 42 | Modi et al40 | F/62 | Abdominal pain | Tail | 2.4 | NI | NI | Cystic lesion | NI | NI | Laparoscopic DP |
| 43 | Fujii et al41 | F/50 | Asymptomatic | Tail | 4 | Unilocular | + | A unilocular cystic lesion with same enhancement as the adjacent spleen | T1 low/T2 high | MCN | Laparoscopic SPDP |
| 44 | Fujii et al41 | F/60 | Back discomfort | Tail | 3.5 | Multilocular | + | A multilocular cystic lesion, solid component with enhancement similar to the spleen | Low T1 and high T2 | IPMN | Laparoscopic DP |
| 45 | Hirabayashi et al42 | M/38 | Asymptomatic | Tail | 3 | Multilocular | Normal | NI | NI | NI | DP |
| 46 | Hirabayashi et al42 | F/40 | Abdominal pain | Tail | 3.5 | Multilocular | + | NI | NI | NI | Enucleation |
| 47 | Hirabayashi et al42 | F/39 | Asymptomatic | Tail | 2 | Multilocular | + | NI | NI | NI | DP |
| 48 | Hirabayashi et al42 | M/54 | Asymptomatic | Tail | 2.7 | Multilocular | Normal | NI | NI | NI | Enucleation |
| 49 | Hirabayashi et al42 | M/55 | Asymptomatic | Tail | 3.5 | Multilocular | + | NI | NI | NI | Enucleation |
| 50 | Hirabayashi et al42 | M/36 | Asymptomatic | Tail | 13.4 | Multilocular | + | NI | NI | NI | DP |
| 51 | Matsumoto et al43 | F/40 | Asymptomatic | Tail | 1.5 | Multilocular | Normal | A multilocular cystic lesion, solid periphery, with the same enhancement as the spleen | High T1- and T2-weighted images | ECIPAS | No |
| 52 | Our patient | M/32 | Asymptomatic | Tail | 3.5 | Multilocular | Normal | A well-defined cystic neoplasm without enhancing mural nodes | NI | MCN | Laparoscopic SPDP |
Note: +, higher than normal.
Abbreviations: CA19-9, carbohydrate antigen 19-9; CT, computed tomography; DP, distal pancreatectomy; DWI, diffusion weighted image; ECIPAS, epidermoid cyst in an intrapancreatic accessory spleen; F, female; IPMN, intraductal papillary mucinous neoplasm; M, male; MCN, mucinous cystic neoplasm; MRI, magnetic resonance imaging; NET, neuroendocrine tumor; NI, no information; PNET, pancreatic neuroendocrine tumor; SPDP, spleen preserving distal pancreatectomy; SPT, solid pseudopapillary tumor; hyper, hyperintensity; hypo, hypointensity.
An elevation of serum CA19-9 level was observed in 21 cases,8,9,13,16–19,22,26,27,29,30,36,37,41,42 and hence, it was difficult to preoperatively differentiate between an ECIPAS and pancreatic malignancy during clinical analysis. Higaki et al8 reported that the serum CA19-9 levels markedly decreased to normal levels after surgery in patients diagnosed with an ECIPAS, a result suggesting that the serum CA19-9 might be secreted from the ECIPAS.
Most cases of ECIPAS are diagnosed after surgical resection based on the pathological characteristics. A preoperative imaging diagnosis of an ECIPAS is extremely difficult. Only 5 cases (9.8%) among the 51 reported cases were diagnosed preoperatively, while 1 out of 5 cases correctly diagnosed preoperatively was followed up without resection. Notably, in the present case, abdominal CT and EUS also revealed pancreatic mucinous neoplasm. As there are no characteristic features to define the lesion on radiology, it is difficult to entirely differentiate the cystic pancreatic malignancy prior to surgery and histopathological examination.
Until now, few studies have reported the imaging characteristics of ECIPAS. Hu et al45 noted that an accessory spleen surrounding the cyst was a key component for correct diagnosis, and therefore the relationship of enhancement between the splenic parenchyma and the parenchymal component of the lesion for the differential diagnosis of a cystic mass in the pancreatic tail was important. Itano et al21 described that 8 of 13 cases showed a solid tumor component upon CT or MRI, and several reports mentioned retrospectively that the images of the solid component were similar to those of the spleen. In our review, a diagnosis of a mucinous cyst-adenoma, cystadenocarcinoma, pseudocyst, neuroendocrine tumor or a potential malignant tumor was suspected in most cases.21 Interestingly, 3 out of 52 cases were diagnosed as ECIPAS preoperatively based on the similar density in the solid component and spleen on CT or MRI.21,37,43 Furthermore, Motosugi et al46 suggested that superparamagnetic iron oxide-based (SPIO) MRI was the most reliable tool for identifying an ECIPAS, because reticuloendothelial tissues including spleen took up SPIO and the signal intensity of the tissues changes (drops). Unfortunately, our patient did not receive MRI examination preoperatively. All the findings suggest that, in the presence of a relatively large amount of splenic tissues, a correct diagnosis would be possible based on a careful examination of images prior to surgery. However, relatively small amounts of splenic tissues may not be useful in the diagnosis. Therefore, ECIPAS should be considered in the differential diagnosis of pancreatic cystic lesions.
Until now, the treatment of ECIPAS consists of follow-up and surgical removal, including open or laparoscopic surgery with or without splenic preservation. No death has been reported during operation or in the short-term postoperative period. Fujii et al41 suggested that laparoscopic distal pancreatectomy could be a useful, minimally invasive surgical approach for treating pancreatic cysts as well as for the treatment of benign or low-grade malignant tumors located in the pancreatic body or tail. As ECIPAS was reported not to have malignant potential, a correct preoperative diagnosis could thereby avoid unnecessary surgery.
Conclusion
An ECIPAS is an extremely rare disease entity. Enhancing the cystic wall of ECIPAS similar to the spleen was a helpful feature. To prevent any unnecessary surgical intervention, it is important to recognize the ECIPAS as the differential diagnosis of pancreatic cyst. Familiarity with the imaging features, the clinical presentation and the location of the cyst will help radiologists make a more confident diagnosis. Thus, making a definite preoperative diagnosis in most cases is possible.
Acknowledgments
This work was supported by grants from the General Research Projects of the Department of Education of Zhejiang Province (No Y201737812), Zhejiang Province Department of Laboratory Animal Science and Technology Plan Projects (No 2018C37115), and Key Research and Development Project of Science and Technology Department of Zhejiang Province (No 2015C03053).
Footnotes
Disclosure
The authors report no conflicts of interest in this work.
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