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浆细胞肿瘤累及胃肠道、肝脏和胰胆系统:116 例回顾性队列的临床病理相关性。

Gastrointestinal, hepatic, and pancreatobiliary involvement by plasma cell neoplasms: clinicopathologic correlations in a retrospective cohort of 116 cases.

机构信息

Department of Pathology, University of Michigan, Ann Arbor, MI, USA.

Department of Pathology, Cleveland Clinic, Cleveland, OH, USA.

出版信息

Histopathology. 2022 Dec;81(6):742-757. doi: 10.1111/his.14778. Epub 2022 Aug 30.

Abstract

AIMS

Plasma cell neoplasms (PCNs) may involve the gastrointestinal (GI) tract in two forms: plasmacytoma (PC), an isolated lesion that lacks marrow involvement, and extramedullary myeloma (EMM). However, previous literature on PCNs involving the GI tract, liver, and pancreas is limited. We evaluated the clinicopathologic features of the largest series of GI PCNs to date.

METHODS AND RESULTS

Six institutional archives were searched for GI, liver, and pancreas cases involved with PCNs. Medical records were reviewed for clinical and imaging features. Histopathologic features evaluated included involved organ, tumor grade, and marrow involvement. Overall, 116 cases from 102 patients were identified. The tumors most presented as incidental findings (29%). The liver was most involved (47%), and masses/polyps (29%) or ulcers (21%) were the most common findings. Most cases had high-grade morphology (55%). The majority (74%) of GI PCNs were classified as EMM due to the presence of marrow involvement at some point during the disease course, occurring within a year of marrow diagnosis in 46% of patients. PC was classified in 26% of patients due to the lack of marrow involvement. Most (70%) patients died from disease within 10 years (median 14.1) of diagnosis and more than half (58%) died within 6 months.

CONCLUSION

PC and EMM involving the GI tract, liver, and pancreas have a wide range of clinicopathologic presentations. Tumors may occur virtually anywhere in the GI tract or abdomen and may precede the diagnosis of marrow involvement. Both GI PC and EMM are associated with a poor prognosis.

摘要

目的

浆细胞瘤(PCN)可通过两种形式累及胃肠道(GI):孤立性病变浆细胞瘤(PC),缺乏骨髓累及,和骨髓外骨髓瘤(EMM)。然而,目前有关 GI 浆细胞瘤、肝脏和胰腺的文献有限。我们评估了迄今为止最大系列 GI 浆细胞瘤的临床病理特征。

方法和结果

从 102 例患者的 102 个机构档案中搜索 GI、肝脏和胰腺涉及 PCN 的病例。对病历进行了回顾,以评估临床和影像学特征。评估的组织病理学特征包括受累器官、肿瘤分级和骨髓累及。总体上,从 102 例患者中确定了 116 例病例。肿瘤最常作为偶然发现(29%)出现。肝脏最常受累(47%),肿块/息肉(29%)或溃疡(21%)是最常见的发现。大多数病例具有高级别形态学(55%)。由于在疾病过程中的某个时间点存在骨髓累及,74%的 GI 浆细胞瘤被归类为 EMM,其中 46%的患者在骨髓诊断后一年内出现骨髓累及。由于缺乏骨髓累及,26%的患者被归类为 PC。70%的患者在诊断后 10 年内(中位 14.1 年)死于疾病,超过一半(58%)的患者在 6 个月内死亡。

结论

累及胃肠道、肝脏和胰腺的 PC 和 EMM 具有广泛的临床病理表现。肿瘤可能发生在胃肠道或腹部的任何部位,并且可能先于骨髓累及的诊断。GI PC 和 EMM 均与预后不良相关。

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