Results 21 to 30 of about 1,427 (174)

A case report of H‐syndrome from Baghdad Medical City treated with tocilizumab

open access: yesClinical Case Reports, Volume 10, Issue 12, December 2022., 2022
H syndrome, also known as histiocytosis‐lymphadenopathy plus syndrome or PHID, is a rare genetic condition caused by mutations in the SLC29A3 gene. This case report presents the first H‐syndrome rarity in Iraq. Abstract This case report presents the first H‐syndrome rarity in Iraq, a 12‐year‐old female patient who was attending the Rheumatology out ...
Nabaa Ihsan Awadh   +6 more
wiley   +1 more source

Intriguing nodules mimicking as leprosy: An interesting case report

open access: yesClinical Dermatology Review, 2023
The differential diagnosis of disseminated infiltrated cutaneous nodules includes a plethora of disorders ranging from the more frequently encountered infective and granulomatous conditions to the obscure ones with proliferative and malignant origin ...
Vasudha A Belgaumkar   +2 more
doaj   +1 more source

Limited sinonasal Rosai–Dorfman disease presenting as chronic sinusitis

open access: yesHistopathology, Volume 81, Issue 1, Page 99-107, July 2022., 2022
A limited form of Rosai‐Dorfman disease can present in the clinical setting of chronic sinusitis. These histologic findings are associated with recurrent chronic sinus symptoms but no risk of systemic disease. Abstract Aims The sinonasal tract is a common extranodal site for Rosai–Dorfman disease (RDD).
Lisa M Rooper   +6 more
wiley   +1 more source

A Rare Case of Multiorgan Involvement of Rosai Dorfman Disease in an Elderly Female

open access: yesJournal of Nepal Medical Association, 2014
Sinus histiocytosis with massive lymphadenopathy (SHML), Rosai-Dorfman Disease, is a rare histiocytic syndrome first described by Rosai and Dorfman, most frequently seen in children and young adults.The disease is more common in males and in individuals ...
Rakesh Digambar Waghmare
doaj   +1 more source

A case report of Rosai–Dorfman disease of the breast

open access: yesJournal of Current Research in Scientific Medicine, 2023
Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a benign, self-limiting disease. In the majority of cases, there is massive and painless lymphadenopathy in any lymph node group but most commonly in the cervical lymph ...
Rini Francis   +3 more
doaj   +1 more source

Rosai-Dorfman Disease: Rare Pulmonary Involvement Mimicking Pulmonary Langerhans Cell Histiocytosis and Review of the Literature

open access: yesCase Reports in Radiology, 2018
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare nonmalignant lymphohistiocytic proliferative disorder.
Rashid AL Umairi   +4 more
doaj   +1 more source

A patient with a papulo‐nodular lesion on the shoulder

open access: yes, 2023
JEADV Clinical Practice, Volume 2, Issue 3, Page 662-665, September 2023.
Fanny Ickx   +4 more
wiley   +1 more source

Rosai-Dorfman disease in a patient with cervical lymphadenopathy and associated Serratia marcescens infection

open access: yesClinical Infection in Practice, 2020
Sinus histiocytosis with massive lymphadenopathy (SHML), also known as Rosai-Dorfman disease (RDD), is a rare idiopathic, non-neoplastic proliferative disorder of histiocytes with an unknown etiology that most often presents as bilateral painless ...
Alvaro E. Galvis   +2 more
doaj   +1 more source

Primary Rosai-Dorfman Disease in 39-Year-Old Woman With Osseous Tibial Lesion Manifestion: A Case Report and Literature Review

open access: yesFoot & Ankle Orthopaedics, 2021
Rosai-Dorfman disease (RDD), otherwise known as sinus histiocytosis with massive lymphadenopathy (SHML), is a very rare and typically benign disorder of unknown etiology with
Jasmin Mansoori DPM   +4 more
doaj   +1 more source

Primary intraosseous manifestation of Rosai-Dorfman disease: 2 cases and review of literature

open access: yesJournal of the Belgian Society of Radiology, 2014
Rosai-Dorman disease (RDD) is a rare disorder of proliferative histiocytes with an unknown etiology. It is also known as sinus histiocytosis with massive lymphadenopathy. Most patients present with painless cervical lymphadenopathy due to accumulation of
H M Duijsens   +4 more
doaj   +1 more source

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