多发性骨髓瘤胆囊浆细胞样浸润表现为急性胆囊炎。

CRSLS : MIS case reports from SLS Pub Date : 2021-08-04 eCollection Date: 2021-10-01 DOI:10.4293/CRSLS.2021.00049
Fadi Alyass, Patrick N Narh-Martey
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引用次数: 0

摘要

继发性远端浆细胞瘤起源于多发性骨髓瘤是一种常见的血液系统恶性肿瘤,表现在疾病的后期。这些浆细胞瘤可引起广泛的全身器官损害。当髓外浆细胞瘤累及胆囊或胆管时,其扩张可表现为急性无结石性胆囊炎或胆管癌。我们报告一例56岁女性IgA κ链多发性骨髓瘤侵袭性病程史,表现为右上腹疼痛伴恶心和呕吐持续一周。她的实验室检查显示肝功能与胆囊病因一致。腹部超声及CT均未见胆结石,排除急性无结石性胆囊炎。最初的医疗管理没有显示任何改善。进行了机器人胆囊切除术,病理检查发现胆囊底肿瘤狭窄,组织学评估显示浆细胞样细胞起源于原发多发性骨髓瘤诊断。手术后患者病情下降,术后表现为转移性肝血栓形成,类似胆管癌,患者后来因姑息治疗而死亡。
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Multiple Myeloma Plasmacytoid Infiltration of the Gallbladder Presenting as Acute Cholecystitis.

Secondary distal plasmacytoma that arise from multiple myeloma is a common hematological malignancy that manifests in later stages of the disease. These plasmacytomas are known to cause extensive systemic organ damage. When extramedullary plasmacytomas reach the gallbladder or biliary ducts, expansion can mimic acute acalculous cholecystitis or cholangiocarcinoma. We report a case of a 56-year-old female with a history of aggressive course IgA κ chain multiple myeloma who presented with right upper quadrant abdominal pain with nausea and vomiting for one week duration. Her laboratory panel revealed liver function tests consistent with gallbladder etiology. Abdominal ultrasound and CT showed no evidence of cholelithiasis precluding to acute acalculous cholecystitis. Initial medical management did not show any improvement. A robotic cholecystectomy was performed, and a pathology review of the specimen found a neoplastic stricture of the gallbladder fundus, the histological evaluation of which revealed plasmacytoid cells originating from her primary multiple myeloma diagnosis. The patient's condition declined following surgery, postoperative presentation included metastatic liver thrombosis mimicking cholangiocarcinoma and the patient later expired with palliative care.

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