Department of General Surgery (Hepatobiliary Surgery), The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Nuclear Medicine and Molecular Imaging Key Laboratory of Sichuan Province, Luzhou, China.
Am Surg. 2023 Jun;89(6):2979-2981. doi: 10.1177/00031348221102606. Epub 2022 May 11.
Castleman disease (CD) is a lymphoproliferative disorder that rarely occurs in the pancreas. We reported a 46-year-old man was admitted to our hospital due to recurrent minor epigastric pain for 7 days. The abdominal enhanced CT showed irregular foci in the body of the pancreas with abundant blood supply considered a neuroendocrine tumor. The patient was subsequently diagnosed with pancreatic neuroendocrine tumor by an ultrasound-guided fine needle aspiration biopsy. Therefore, he underwent an open pancreatic mass resection. The ultimate diagnosis was CD and belonged to hyaline vascular type based on the postoperative pathology. After a 13-month follow-up, no recurrence of abdominal pain or lesions was observed. This case suggests that fine needle aspiration biopsy is not conclusive and unsuitable for pancreatic CD and highlights the importance of routine pathology due to the absence of typical signs and symptoms.
Castleman 病(CD)是一种罕见发生于胰腺的淋巴组织增生性疾病。我们报告了 1 例 46 岁男性,因反复上腹痛 7 天入院。腹部增强 CT 显示胰腺体部不规则病灶,血供丰富,考虑神经内分泌肿瘤。患者随后经超声引导下细针抽吸活检诊断为胰腺神经内分泌肿瘤。因此,行开腹胰腺肿块切除术。术后病理最终诊断为 CD,属于透明血管型。术后 13 个月随访,未观察到腹痛或病灶复发。本例提示细针抽吸活检不具确定性,不适合胰腺 CD,强调由于缺乏典型症状和体征,常规病理的重要性。