About 730 results

ALLMedicine™ Rosai-Dorfman Disease Center

Research & Reviews  285 results

Rosai-Dorfman Disease of the Chest Wall Following Mastectomy for Breast Cancer.
The American Surgeon; Merrell MA, Grenn EE et. al.

May 6th, 2022 - Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder generally affecting the cervical lymph nodes as sinus histiocytosis with massive lymphadenopathy. We present a unique case of multifocal soft tissue RDD originating fr...

Primary Rosai-Dorfman disease of the thymus and lung: A clinicopathological and immunoh...
Pathology, Research and Practice; Oramas DM, Moran CA

May 1st, 2022 - Three cases of primary Rosai-Dorfman disease of the thymus and lung are presented. The patients are 3 men between the ages of 42 and 47 years who presented with non-specific symptoms including cough, chest pain, and shortness of breath. Clinically...

Orbital Rosai-Dorfman Disease Presenting as Optic Neuritis.
Journal of Neuro-ophthalmology : the Official Journal of ... Virk HS, Shahlaie K et. al.

Apr 28th, 2022 - Orbital Rosai-Dorfman Disease Presenting as Optic Neuritis.|2022|Virk HS,Shahlaie K,Ramani B,Perry A,Fragoso R,|complications,diagnosis,diagnosis,etiology,

Management of central nervous system Rosai-Dorfman disease: A single center treatment e...
Journal of Clinical Neuroscience : Official Journal of Th... Zhu Q, Liang Y et. al.

Mar 25th, 2022 - Rosai-Dorfman disease (RDD) is an idiopathic histiocytic proliferation disease with various clinical manifestations. A retrospective study of patients with pathological diagnosed RDD primarily involved in the central nervous system was conducted f...

Rosai-Dorfman disease mimicking subdural hematoma: a case report.
The Journal of International Medical Research; Zhou Z, Jian S et. al.

Mar 15th, 2022 - Rosia-Dorfman disease (RDD) is a rare benign disease with exceedingly rare neural involvement. In this report, we describe a very rare case of intracranial RDD mimicking a subdural hematoma. The patient presented with headache and a suspected hist...

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Guidelines  1 results

The Mayo Clinic Histiocytosis Working Group Consensus Statement for the Diagnosis and E...
Mayo Clinic Proceedings; Goyal G, Young JR et. al.

Sep 2nd, 2019 - Histiocytic neoplasms, a rare and heterogeneous group of disorders, primarily include Erdheim-Chester disease, Langerhans cell histiocytosis, and Rosai-Dorfman disease. Due to their diverse clinical manifestations, the greatest challenge posed by ...

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Clinicaltrials.gov  3 results

Cobimetinib in Refractory Langerhans Cell Histiocytosis (LCH), and Other Histiocytic Disorders

Sep 2nd, 2021 - Histiocytic disorders are diseases caused by misfunctioning or buildup of particular immune cells called histiocytes. Many histiocytic disorders (LCH, juvenile xanthogranuloma (JXG), Erdheim-Chester disease (ECD), and Rosai-Dorfman Disease (RDD)) ...

Lenalidomide and Dexamethasone for Rosai-Dorfman Disease

Jun 16th, 2021 - Rosai-Dorfman Disease (RDD) is a rare, heterogeneous histiocytic disorder. Because of the rarity of RDD and a lack of prospective randomized trials, the treatment strategy for RDD is mostly based on retrospective study. Steroid was suggested as fr...

International Rare Histiocytic Disorders Registry (IRHDR)

Mar 9th, 2021 - Histiocytoses are rare diseases caused by an excess of cells called Histiocytes, which can infiltrate the skin, bones, lungs, liver, spleen and the central nervous system. These disorders can range from localized involvement that resolves spontane...

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News  3 results

A 42-Year-Old Man With a Right Ear Mass

Jul 30th, 2015 - The appearance of extranodal manifestations of Rosai-Dorfman disease has been limited to case reports, and there have been only three other cases involving the ear. These involved bilateral cauliflower ears,[4] middle ear or external auditory cana...

Rosai-Dorfman Disease
Alyssa Miceli, DO, Nathan Cleaver, DO et. al.

Jul 9th, 2015 - Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare benign histioproliferative disorder of unknown etiology. 1 Clinically, it is most frequently characterized by massive painless cervical lymphaden.

Necrobiosis Lipoidica Diabeticorum
Adam S. Richardson, BS, Eric W. Hossler, MD

May 12th, 2015 - Necrobiosis lipoidica diabeticorum (NLD) is a rare granulomatous skin manifestation that is strongly associated with diabetes mellitus. Necrobiosis lipoidica diabeticorum is more common among females and occurs primarily in the pretibial area.

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