Rosai-Dorfman Disease: A Rare Disease with Uncommon 18F-FDG PET CT Findings.

IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Indian Journal of Nuclear Medicine Pub Date : 2025-07-01 Epub Date: 2025-09-19 DOI:10.4103/ijnm.ijnm_21_25
T Kishan Subudhi, Ashique Rahman, Saitej Reddy, Kanhaiyalal Agrawal, Ashutosh Panigrahi, Girish Kumar Parida
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引用次数: 0

Abstract

Rosai-Dorfman disease (RDD) also called as sinus histiocytosis with lymphadenopathy is a rare benign histiocytic proliferative disorder of unknown etiology and was first described in 1969 with the incidence of 1 in 200,000. Most commonly present with lymphadenopathy with around 40 percent presented with extranodal involvement such as skin, central nervous system, nasal cavity, and bones. Bone involvement is rare and it is <10% cases of RDD. We present a case of RDD with extranodal involvement such as nasal cavity, cutaneous nodules, paraspinal lesion with intraspinal extension, and uncommon appendicular skeleton involvement (tibia and fibular involvement).

Rosai-Dorfman病:一种罕见的18F-FDG PET CT表现。
rossai - dorfman病(RDD)也称为窦性组织细胞增生伴淋巴结病,是一种病因不明的罕见良性组织细胞增生疾病,于1969年首次报道,发病率为20万分之一。最常见的表现为淋巴结病变,约40%表现为淋巴结外受累,如皮肤、中枢神经系统、鼻腔和骨骼。骨受累是罕见的,它是
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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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