FDG PET Scan in Cutaneous Rosai-Dorfman-Destombes Disease.

IF 0.4 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Indian Journal of Nuclear Medicine Pub Date : 2024-09-01 Epub Date: 2025-01-25 DOI:10.4103/ijnm.ijnm_121_24
Shrikant Vasantrao Solav, Chakor Vora, Rajlaxmi Jagtap, Shailendra Savale, Ishtiyaq Shaikh, Aman Solav
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引用次数: 0

Abstract

Rosai-Dorfman-Destombes (RDD) disease is also called as sinus histiocytosis and is characterized by enlarged lymph nodes and previously called as non-Langerhans cell histiocytosis. Based on pathologic, molecular, and genetic features, RDD disease has been classified into sporadic noncutaneous (classical nodal, extranodal, neoplasia associated, and autoimmune associated), familial (H syndrome, autoimmune lymphoproliferative syndrome related, and familial NOS), and cutaneous subtypes. Cutaneous RDD disease is not associated with lymphadenopathy or visceral organ involvement. The disease is usually localized and has relatively better long-term prognosis. Presented here is a case of indurated plaque-like skin lesions over the abdomen. 18F-fluorodeoxyglucose (FDG) positron emission tomography-computed tomography scan revealed FDG avid cutaneous-subcutaneous soft-tissue lesions. Histology confirmed the diagnosis of cutaneous RDD disease.

FDG PET扫描在皮肤Rosai-Dorfman-Destombes病中的应用。
rossai - dorfman - destombes (RDD)病也被称为窦性组织细胞增多症,其特征是淋巴结肿大,以前被称为非朗格汉斯细胞组织细胞增多症。基于病理、分子和遗传特征,RDD疾病被分为散发性非皮肤型(经典淋巴结、结外、肿瘤相关和自身免疫性相关)、家族性(H综合征、自身免疫性淋巴增生性综合征相关和家族性NOS)和皮肤亚型。皮肤RDD疾病与淋巴结病或脏器受累无关。这种疾病通常是局部的,长期预后相对较好。这是一个腹部硬化斑块样皮肤病变的病例。18f -氟脱氧葡萄糖(FDG)正电子发射断层扫描-计算机断层扫描显示FDG强烈的皮肤-皮下软组织病变。组织学证实了皮肤RDD疾病的诊断。
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来源期刊
Indian Journal of Nuclear Medicine
Indian Journal of Nuclear Medicine RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
CiteScore
0.70
自引率
0.00%
发文量
46
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