F-fluoro-2-deoxyglucose Positron Emission-computed Tomography in a Rare Cutaneous Form of Rosai-Dorfman Disease: A Case Report

Overview

Journal Mol Clin Oncol

Specialty Oncology

Date 2018 Feb 14

PMID 29435284

Citations 4

Authors

Joya Hadchiti

Francois G Kamar

Jean Abi Ghosn

Mohamad Haidar

Ahmad Younes

Antoine Obeid

Marwan Haddad

Fadi Farhat

Feras Chehade

Affiliations

Soon will be listed here.

Abstract

Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, commonly involves the lymph nodes but may secondarily involve the skin. Purely cutaneous disease without lymphatics or internal organ involvement occurs rarely. The present report detailed a rare case of F-fluoro-2-deoxyglucose positron emission-computed tomography (FDG PET-CT) performed in a 33-year-old male soldier with a purely cutaneous form of RDD. Staging with FDG PET-CT was ordered prior to excisional biopsies of the aforedescribed masses and pathology reported RDD. The case demonstrated accurate localization of increased radioglucose metabolism. The present case was also discussed in light of literature data in terms of clinical features, etiologies, histology, medical imaging, therapy planning and prognosis.

Citing Articles

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Three Cases of Extranodal Rosai-Dorfman Disease and Literature Review.

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Primary Cutaneous Rosai-Dorfman Disease of the Scalp.

Mizuta H, Nakano E, Yamazaki N Dermatol Pract Concept. 2020; 11(1):e2020086.

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