Results 21 to 30 of about 1,868 (215)

Prednisone and Vincristine for the Treatment of Pediatric Rosai-Dorfman Disease: A Case Report. [PDF]

open access: yesCase Rep Med
Purpose Pediatric Rosai–Dorfman disease (RDD) is extremely rare, and the current treatment plan is not unified. We hope that our study provides new ideas for the clinical treatment of RDD. Methods We report a case in which RDD was successfully treated with prednisone and vincristine, resulting in regression of enlarged lymph nodes.
Dun J, Hu Q, Liu A, Wang Y, Zhang A.
europepmc   +2 more sources

Sinus Histiocytosis: An Uncommon Presentation of an Uncommon Condition [PDF]

open access: yes, 2015
Introduction Rosai–Dorfman Disease (RDD), also known as Sinus Histiocytosis with Massive Lymphadenopathy (SHML), is a rare, benign, proliferative disorder of macrophages and monocytes that was first described by Rosai and Dorfman in 1969.
Greco, MD, Allison, Kane, MD, Gregory
core   +2 more sources

Bilateral breast Rosai‐Dorfman disease screen detected by mammography

open access: yesClinical Case Reports, Volume 11, Issue 3, March 2023., 2023
Rosai‐Dorfman disease (RDD) is a rare proliferative disorder of histiocytes typically found in nodal sites, however, it can also present initially as an asymptomatic mass in the breast. Presenting symptoms may include fever, lymphadenopathy, and weight loss. Tissue sampling is definitive for diagnosis and close surveillance is recommended.
Christina Sumner   +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

Langerhans Cell Histiocytosis of the Uvea with a Ciliochoroidal Mass: A Case Report of Management with Systemic Therapy

open access: yesCase Reports in Ophthalmological Medicine, Volume 2023, Issue 1, 2023., 2023
Background. This study is aimed at exploring a case of choroidal Langerhans cell histiocytosis (LCH) successfully treated with systemic corticosteroid and immunosuppressant. Case presentation. A 24‐year‐old man with known multisystem LCH developed loss of vision, ocular pain, conjunctival injection, panuveitis, and a ciliochoroidal mass.
Fariba Ghassemi   +5 more
wiley   +1 more source

Unusual presentation of Rosai-Dorfman disease in a 14-month-old Italian child: a case report and review of the literature [PDF]

open access: yes, 2016
Background: Rosai-Dorfman disease (RDD) is a rare form of histiocytosis characterized by histiocyte proliferation within lymph nodes and extranodal tissue. Here we report an unusual presentation of RDD in an Italian toddler.
Bruzzi, Patrizia   +5 more
core   +2 more sources

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

Asymptomatic flow of Rosai-Dorfman disease [PDF]

open access: yes, 2014
Introduction. Sinus histiocytosis with massive lymphadenopathy is a rare benign self-limiting disease of unknown etiology. The salivary gland involvement, indicating the extranodal character of the disease, often presents a diagnostic dilemma ...
Bjelaković Bojko   +10 more
core   +1 more source

A Rare Case of a Systemic Non-Langerhans Histiocytosis Presenting with Diabetes Insipidus and a Tentorial Mass [PDF]

open access: yes, 2015
Introduction The histiocytoses are a group of clinically diverse diseases distinguished from one another based on the specific immunophenotype of the lesional cells, implying derivation from the same precursor cell.
Barros, MS, Guilherme   +5 more
core   +2 more sources

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