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皮下脂膜炎样T细胞淋巴瘤的放射学和临床特征

Radiological and clinical features of subcutaneous panniculitis-like T-cell lymphoma.

作者信息

Kim Jong Woo, Chae Eun Jin, Park Young Soo, Lee Hyun Joo, Hwang Hye Jeon, Lim Chaehun, Chung Hye Won

机构信息

Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.

出版信息

J Comput Assist Tomogr. 2011 May-Jun;35(3):394-401. doi: 10.1097/RCT.0b013e3182106585.

Abstract

OBJECTIVE

To retrospectively analyze computed tomography (CT) and clinical findings of patients with subcutaneous panniculitis-like T-cell lymphoma (SPTCL).

MATERIALS AND METHODS

The CT findings were retrospectively assessed in 8 patients (6 men, 2 women; age range, 23-60 years; mean age, 39.8 years) with pathologically proven SPTCL. The tumor location, number, distribution, size, and morphological characteristics on CT were evaluated, as were maximum standardized uptake values on positron emission tomography. We also evaluated patient symptoms, laboratory findings, immunophenotype, involvement of bone marrow, treatment, and outcomes.

RESULTS

All 8 patients had multiple (range, 4 to numerous) soft tissue lesions involving subcutaneous fat tissue of the chest, abdominal wall, back, and buttock. Lesions varied in size (range, 0.5-10 cm) and showed reticular (n = 1), nodular (n = 4), and diffuse infiltrative (n = 3) patterns. Three patients had lesions involving the entire thickness of fat tissue, 3 had partial lesions, and 2 had variable lesions. Skin thickening was mild in 4 patients, moderate in 2, and severe in 2; fascia thickening was mild in 3 patients, moderate in one, severe in one, and variable in 2. In 7 patients, lesions were accompanied by engorged supplying vessels. At onset, maximum standardized uptake values varied from 1.2 to 4.7, decreasing to 0.0 to 4.2. Five patients had αβ type and one had γδ type. Clinical outcome varied: two remain alive with disease, two had no disease, and one died.

CONCLUSIONS

The SPTCL is characterized by multiple, nodular, or diffuse soft tissue lesions involving subcutaneous fat tissue, accompanied by engorged vessels and skin and fascial thickening. Patients vary in presentation and in treatment outcomes.

摘要

目的

回顾性分析皮下脂膜炎样T细胞淋巴瘤(SPTCL)患者的计算机断层扫描(CT)及临床特征。

材料与方法

回顾性评估8例经病理证实的SPTCL患者(6例男性,2例女性;年龄范围23 - 60岁;平均年龄39.8岁)的CT表现。评估肿瘤在CT上的位置、数量、分布、大小及形态特征,以及正电子发射断层扫描的最大标准化摄取值。我们还评估了患者的症状、实验室检查结果、免疫表型、骨髓受累情况、治疗及预后。

结果

所有8例患者均有多个(范围4个至多个)软组织病变,累及胸部、腹壁、背部及臀部的皮下脂肪组织。病变大小各异(范围0.5 - 10 cm),表现为网状(n = 1)、结节状(n = 4)及弥漫浸润性(n = 3)。3例患者病变累及脂肪组织全层,3例为部分病变,2例为多变病变。4例患者皮肤增厚轻度,2例中度,2例重度;3例患者筋膜增厚轻度,1例中度,1例重度,2例多变。7例患者病变伴有供血血管增粗。发病时,最大标准化摄取值为1.2至4.7,治疗后降至0.0至4.2。5例为αβ型,1例为γδ型。临床预后各异:2例带瘤生存,2例无病生存,1例死亡。

结论

SPTCL的特征为累及皮下脂肪组织的多个结节状或弥漫性软组织病变,伴有血管增粗及皮肤和筋膜增厚。患者的表现及治疗结果各不相同。

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