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骨髓瘤中的广泛髓外疾病。一种具有预后不良和去分化特征的罕见变体。

Extensive extramedullary disease in myeloma. An uncommon variant with features of poor prognosis and dedifferentiation.

作者信息

Sanal S M, Yaylaci M, Mangold K A, Pantazis C G

机构信息

Department of Medicine, Medical College of Georgia, Augusta 30912-3125, USA.

出版信息

Cancer. 1996 Apr 1;77(7):1298-302. doi: 10.1002/(SICI)1097-0142(19960401)77:7<1298::AID-CNCR11>3.0.CO;2-X.

Abstract

BACKGROUND

The development of extramedullary plasmacytomas and elevated serum lactic dehydrogenase (LDH) in myeloma indicates poor prognosis. A 75-year-old man was diagnosed with immunoglobulin (Ig) A, lambda myeloma when he developed pathologic rib fractures, hypercalcemia, and anemia. After 6 months of treatment with melphalan and prednisone, he was in complete remission as evidenced by the disappearance of the monoclonal protein in the serum and free light chain in the urine. Eight months after diagnosis, his disease took an unusual course with the simultaneous development of plasmacytomas in the skin, breast, stomach, and pancreatic head, complicated by severe upper gastrointestinal bleeding and obstructive jaundice.

METHODS

Immunohistochemical staining of the marrow and breast mass was done using monoclonal antibodies against B-cell and T-cell antigens as well as kappa and lambda light chains. In situ hybridization was performed to detect ras oncogene overexpression in the breast mass.

RESULTS

Immunohistochemical staining of the original marrow and breast mass was positive for IgA and lambda, confirming the identical clonal origin of the plasma cells. The disorder expressed elevated serum LDH, both at diagnosis and relapses. Features of dedifferentiation were expressed by the disappearance of myeloma protein in the serum at relapse, absence of marrow plasma cell infiltration, and development of multiple extramedullary plasmacytomas. There was no overexpression of H-ras or N-ras oncogenes by in situ hybridization of the plasmacytoma from the breast. The patient died shortly after the development of the extramedullary plasmacytomas.

CONCLUSIONS

The simultaneous appearance of plasmacytomas in multiple extramedullary sites heralds a change of clinical behavior in myeloma. When accompanied by the disappearance of serum myeloma protein, and marrow plasma cell infiltration, and serum LDH elevation, the disorder may follow a fulminant course.

摘要

背景

髓外浆细胞瘤的发生以及骨髓瘤患者血清乳酸脱氢酶(LDH)升高提示预后不良。一名75岁男性在出现病理性肋骨骨折、高钙血症和贫血时被诊断为免疫球蛋白(Ig)Aλ型骨髓瘤。在接受美法仑和泼尼松治疗6个月后,他达到完全缓解,血清中单克隆蛋白和尿中游离轻链消失可资证明。诊断8个月后,他的病情出现异常变化,皮肤、乳腺、胃和胰头同时出现浆细胞瘤,并伴有严重的上消化道出血和梗阻性黄疸。

方法

使用针对B细胞和T细胞抗原以及κ和λ轻链的单克隆抗体对骨髓和乳腺肿块进行免疫组织化学染色。进行原位杂交以检测乳腺肿块中ras癌基因的过表达。

结果

原始骨髓和乳腺肿块的免疫组织化学染色显示IgA和λ呈阳性,证实浆细胞具有相同的克隆起源。该疾病在诊断和复发时血清LDH均升高。复发时血清骨髓瘤蛋白消失、骨髓浆细胞浸润缺失以及多发性髓外浆细胞瘤的出现均表现出去分化特征。乳腺浆细胞瘤的原位杂交未显示H-ras或N-ras癌基因过表达。该患者在髓外浆细胞瘤出现后不久死亡。

结论

多发性髓外部位同时出现浆细胞瘤预示着骨髓瘤临床行为的改变。当伴有血清骨髓瘤蛋白消失、骨髓浆细胞浸润以及血清LDH升高时,该疾病可能呈暴发性病程。

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