Results 11 to 20 of about 1,868 (215)

A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations

open access: yesJournal of Cutaneous Immunology and Allergy, 2023
Rosai–Dorfman disease (RDD) is a rare non‐Langerhans cell histiocytosis that was first described as sinus histiocytosis with massive lymphadenopathy by Rosai and Dorfman in 1969.
Shintaro Saito   +3 more
doaj   +2 more sources

The Clinicopathologic Spectrum of Rosai-Dorfman-Destombes Disease in Adults: An Analysis of 16 Cases. [PDF]

open access: yesEur J Haematol
ABSTRACT Rosai–Dorfman–Destombes disease (RDD) is a rare histiocytic proliferation with protean clinical manifestations, resulting from the accumulation of activated histiocytes within nodal and extra‐nodal tissues. The diagnosis can be missed, particularly when biopsies are obtained from extra‐nodal sites, where histological features may be less ...
Trinder M   +8 more
europepmc   +2 more sources

Sinus Histiocytosis with Massive Lymphadenopathy [PDF]

open access: yesCA: A Cancer Journal for Clinicians, 1980
A 22-month-old child presented with massive cervical adenopathy accompanied by a retropharyngeal mass that caused stridor and dysphagia. Biopsy from both sides was consistent with sinus histiocytosis with massive lymphadenopathy (SHML). SHML is an unusual benign lesion that characteristically presents with painless, massive cervical adenopathy ...
J, Dearth, D, Hunter, D, Kelly, W, Crist
openaire   +2 more sources

Sinus Histiocytosis with Massive Lymphadenopathy [PDF]

open access: yesLeukemia & Lymphoma, 1992
To date, the morphological aspects of sinus histiocytosis with massive lymphadenopathy (SHML) have been fully described. The disease is characterized by an enlargement of lymph nodes in which the sinuses are dilated and infiltrated by histiocytes, often phagocytosing lymphocytes.
SACCHI, Stefano   +3 more
openaire   +5 more sources

Rosai‐Dorfman disease in 6‐year‐old child: Presentation, diagnosis, and treatment

open access: yesClinical Case Reports, 2021
Rosai‐Dorfman disease is referred to as sinus histiocytosis massive lymphadenopathy. We are reporting a rare case of Rosai‐Dorfman disease, a case of 6‐year‐old boy with a history of multiple painless submandibular and cervical lymphadenopathy.
Kalpana Giri   +3 more
doaj   +1 more source

Rosai–Dorfman disease presenting as internal jugular vein thrombosis and middle lobe collapse-consolidation

open access: yesLung India, 2020
Rosai–Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy, is a rare and benign disease that usually presents as massive and painless cervical lymphadenopathy.
Ambika Sharma   +5 more
doaj   +1 more source

Rosai-Dorfman Disease, Presenting as a Mass in the Trachea: A Case Report. [PDF]

open access: yesRespirol Case Rep
We present a rare case of Rosai–Dorfman disease (RDD) confined solely to the trachea. After initial bronchoscopic resection, systemic corticosteroid therapy was initiated due to lesion progression, successfully stabilizing the disease for 4 years. ABSTRACT A 45‐year‐old woman was referred to our clinic for evaluation of a 17 mm tracheal mass detected ...
Youn T, Lee B, Han J, Jeong BH.
europepmc   +2 more sources

A comparison of the International Consensus and 5th WHO classifications of T‐cell lymphomas and histiocytic/dendritic cell tumours

open access: yesBritish Journal of Haematology, Volume 203, Issue 3, Page 369-383, November 2023., 2023
The simultaneous existence of two classifications of haemato‐lymphoid tumours poses problems not only for diagnosis formulation but also for patients' management and design of clinical trials. Summary Since the publication in 2017 of the revised 4th Edition of the World Health Organization (WHO) classification of haematolymphoid tumours, here referred ...
Brunangelo Falini   +2 more
wiley   +1 more source

Orbital involvement in Rosai-Dorfman disease [PDF]

open access: yes, 2011
A doença de Rosai-Dorfman (DRD) ou histiocitose sinusal com linfadenopatia maciça é uma entidade clínica idiopática, rara e benigna, caracterizada pela proliferação histiocitária com linfofagocitose. Geralmente se apresenta com linfoadenomegalia cervical,
GONÇALVES, Allan C. Pieroni   +4 more
core   +2 more sources

Patient with Rosai-Dorfman-Destombes disease: 18F-FDG-PET/CT scan as a diagnostic tool

open access: yesActa Médica Peruana, 2023
Rosai-Dorfman-Destombes disease (RDD) is a rare non-Langerhans cell histiocytosis, with sinus involvement and massive lymphadenopathy. RDD is usually self-limited; it can appear alone or related to other diseases. We present a 9-year-old male with biopsy
Luis C. Araujo Cachay
doaj   +1 more source

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