Tanaka F, Mori M, Haraguchi M, Makino N, Yoshikawa Y, Akiyoshi T
Department of Surgery, Medical Institute of Bioregulation, Kyushu University, Beppu, Japan.
Surg Today. 1999;29(1):80-2. doi: 10.1007/BF02482976.
We herein report on a 62-year-old man who developed extraadrenal pheochromocytoma and von Meyenberg complexes of the liver (bile duct microhamartoma). The patient identified preoperatively as having a paraaortic mass which was subsequently diagnosed to be a pheochromocytoma. During the operation, small multiple nodules were unexpectedly recognized in the liver. Some of the liver nodules were resected by a wedge biopsy, and then were pathologically identified to be von Meyenberg complexes. This may be the first reported case of the coexistence of pheochromocytoma and von Meyenberg complexes. It is therefore necessary for surgeons to be aware of von Meyenberg complexes in the differential diagnosis of multiple liver metastases in malignant disease.
我们在此报告一名62岁男性,其患有肾上腺外嗜铬细胞瘤和肝脏的梅耶尔堡复合体(胆管微错构瘤)。该患者术前被确定为主动脉旁有肿物,随后被诊断为嗜铬细胞瘤。手术过程中,意外发现肝脏内有多个小结节。部分肝脏结节通过楔形活检切除,随后经病理鉴定为梅耶尔堡复合体。这可能是首例报道的嗜铬细胞瘤与梅耶尔堡复合体并存的病例。因此,外科医生在恶性疾病多发肝转移的鉴别诊断中需要注意梅耶尔堡复合体。