Ulrich J D, Specht K, Schlitter A M, Ceyhan G O, Quante M, Schmid R M, Schlag C
Klinik und Poliklinik für Innere Medizin II, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany.
Institut für Allgemeine Pathologie und Pathologische Anatomie, Technische Universität München, Munich, Germany.
Endosc Int Open. 2020 Jan;8(1):E25-E28. doi: 10.1055/a-1038-3852. Epub 2020 Jan 8.
A 49-year-old woman consulted her general practitioner (GP) regarding epigastric pain that she had experienced for 2 months. Physical examination and laboratory results were unremarkable. An abdominal ultrasound indicated a solid pancreatic tumor, which was confirmed on subsequent CT and MRI. Endoscopic ultrasound (EUS) showed a well-defined heterogeneous, predominantly hypoechoic mass in the pancreatic body, so a neuroendocrine tumor (NET) was suspected. However, EUS-guided fine-needle aspiration (EUS-FNA) was performed and based on (immuno-)histochemical findings, the extremely rare diagnosis of a perivascular epithelioid cell tumor (PEComa) of the pancreas was made. Due to the malignant potential of pancreatic PEComas, laparoscopic left-sided pancreatectomy was performed. We present a case diagnosed by preoperative EUS-FNA highlighting the clinical and endosonographic features which help to distinguish it from its most important differential diagnosis, neuroendocrine tumors (NETs) of the pancreas.
一名49岁女性因上腹部疼痛2个月而咨询其全科医生(GP)。体格检查和实验室检查结果均无异常。腹部超声显示胰腺有一个实性肿瘤,随后的CT和MRI证实了这一点。内镜超声(EUS)显示胰体部有一个边界清晰的不均匀、以低回声为主的肿块,因此怀疑是神经内分泌肿瘤(NET)。然而,进行了EUS引导下细针穿刺(EUS-FNA),并根据(免疫)组织化学结果,做出了胰腺血管周上皮样细胞瘤(PEComa)这一极其罕见的诊断。由于胰腺PEComa具有恶性潜能,遂进行了腹腔镜左侧胰腺切除术。我们报告一例经术前EUS-FNA诊断的病例,重点介绍有助于将其与最重要的鉴别诊断——胰腺神经内分泌肿瘤(NET)相区分的临床和内镜超声特征。