{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,25]],"date-time":"2026-05-25T08:05:54Z","timestamp":1779696354670,"version":"3.53.1"},"reference-count":6,"publisher":"Scientific Scholar","issue":"4","license":[{"start":{"date-parts":[[2025,7,1]],"date-time":"2025-07-01T00:00:00Z","timestamp":1751328000000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2025,7]]},"abstract":"<jats:p>Rosai\u2013Dorfman 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 &lt;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).<\/jats:p>","DOI":"10.4103\/ijnm.ijnm_21_25","type":"journal-article","created":{"date-parts":[[2025,9,19]],"date-time":"2025-09-19T14:00:20Z","timestamp":1758290420000},"page":"261-262","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["Rosai\u2013Dorfman Disease: A Rare Disease with Uncommon 18F-FDG PET CT Findings"],"prefix":"10.25259","volume":"40","author":[{"given":"T. Kishan","family":"Subudhi","sequence":"first","affiliation":[{"name":"Department of Nuclear Medicine, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ashique","family":"Rahman","sequence":"additional","affiliation":[{"name":"Department of Nuclear Medicine, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Saitej","family":"Reddy","sequence":"additional","affiliation":[{"name":"Department of Nuclear Medicine, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kanhaiyalal","family":"Agrawal","sequence":"additional","affiliation":[{"name":"Department of Nuclear Medicine, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ashutosh","family":"Panigrahi","sequence":"additional","affiliation":[{"name":"Department of Haematology, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Girish Kumar","family":"Parida","sequence":"additional","affiliation":[{"name":"Department of Nuclear Medicine, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"10894","published-online":{"date-parts":[[2025,9,19]]},"reference":[{"key":"R1-20250922","first-page":"304","article-title":"Intracranial ROSAI-DORFMAN disease","volume":"17","author":"Mahzoni","year":"2012","journal-title":"J Res Med Sci"},{"issue":"Suppl 1","key":"R2-20250922","first-page":"1336","article-title":"Rosai-Dorfman diseas \u2013 Typical and atypical FDG-PET\/CT findings","volume":"55","author":"Martineau","year":"2014","journal-title":"J Nucl Med"},{"key":"R3-20250922","doi-asserted-by":"crossref","first-page":"268","DOI":"10.1097\/RLU.0b013e31828731da","article-title":"18F-FDG PET\/CT imaging features of Rosai Dorfman disease: A rare cause of massive generalized lymphadenopathy","volume":"39","author":"Karunanithi","year":"2014","journal-title":"Clin Nucl Med"},{"key":"R4-20250922","first-page":"19","article-title":"Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): Review of the entity","volume":"7","author":"Foucar","year":"1990","journal-title":"Semin Diagn Pathol"},{"key":"R5-20250922","doi-asserted-by":"crossref","first-page":"2877","DOI":"10.1182\/blood-2018-03-839753","article-title":"Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease","volume":"131","author":"Abla","year":"2018","journal-title":"Blood"},{"key":"R6-20250922","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1007\/s11926-017-0656-6","article-title":"Bone involvement in Rosai-Dorfman disease (RDD): A case report and systematic literature review","volume":"19","author":"Mosheimer","year":"2017","journal-title":"Curr Rheumatol Rep"}],"container-title":["Indian Journal of Nuclear Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.lww.com\/10.4103\/ijnm.ijnm_21_25","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,5,25]],"date-time":"2026-05-25T07:38:32Z","timestamp":1779694712000},"score":1,"resource":{"primary":{"URL":"https:\/\/ijnm.co.in\/rosaidorfman-disease-a-rare-disease-with-uncommon-18f-fdg-pet-ct-findings\/"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,7]]},"references-count":6,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2025]]}},"URL":"https:\/\/doi.org\/10.4103\/ijnm.ijnm_21_25","relation":{},"ISSN":["0972-3919","0974-0244"],"issn-type":[{"value":"0972-3919","type":"print"},{"value":"0974-0244","type":"electronic"}],"subject":[],"published":{"date-parts":[[2025,7]]},"assertion":[{"value":"2025-02-11","name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2025-04-02","name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}}]}}