埃尔德海姆-切斯特病表现为双侧乳房凹陷和变色

Q4 Medicine
Christina Oska DO , Ujas Parikh MD
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引用次数: 0

摘要

埃尔德海姆-切斯特病是一种以组织细胞异常增殖为特征的罕见疾病。最常受影响的部位是长骨,而乳房受累则非常罕见。在乳房受累的患者中,单侧乳房肿块是最常见的表现。我们介绍了一例独特的埃尔德海姆-切斯特氏病病例,患者为一名 45 岁女性,最初表现为双侧乳房弥漫性凹陷和红斑。临床表现类似炎性乳腺癌,伴有弥漫性乳房凹陷、红斑和相关乳房肿块,不同之处在于双侧乳房均受累。通过乳腺影像诊断和组织病理学检查,采用多学科综合方法诊断和治疗埃尔德海姆-切斯特病。厄德海姆-切斯特病虽然罕见,但在乳房非典型病变的鉴别诊断中应加以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Erdheim Chester disease presenting as bilateral breast dimpling and discoloration
Erdheim Chester disease is a rare disease characterized by abnormal proliferation of histiocytes. The most commonly affected site is the long bones, while involvement of the breasts is very rare. In patients with breast involvement, a unilateral breast mass is the most common presentation. We present a unique case of Erdheim Chester Disease initially presenting as diffuse, bilateral breast dimpling and erythema in a 45-year-old female. Clinically, the presentation mimicked inflammatory breast carcinoma with diffuse breast dimpling, erythema, and associated breast masses, and differing in that both breasts were involved. Diagnostic breast imaging and histopathology led to a comprehensive multidisciplinary approach to diagnosis and management of Erdheim Chester Disease. Although rare, Erdheim Chester Disease should be considered in the differential diagnosis of atypical breast lesions.
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来源期刊
Radiology Case Reports
Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.10
自引率
0.00%
发文量
1074
审稿时长
30 days
期刊介绍: The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.
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