Characteristics of histiocytic neoplasms presenting as breast masses. [PDF]
Br J HaematolBritish Journal of Haematology, Volume 208, Issue 1, Page 358-362, January 2026.
Vougiouklakis T +10 more
europepmc +2 more sources
Patient with Rosai-Dorfman-Destombes disease: 18F-FDG-PET/CT scan as a diagnostic tool
Acta 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
Tumoral Stage of Mycosis Fungoides, Misdiagnosed With Wells Syndrome and Langerhans Cell Histiocytosis Histologically: A Challenging Case and Review of the Literature. [PDF]
Cancer Rep (Hoboken)ABSTRACT Background Mycosis fungoides (MF) is a type of cutaneous T‐cell lymphoma (CTCL) with slow progression, usually presenting with patches and plaques. The infiltration of histiocytes and eosinophils in skin cancers can mask the underlying condition, posing a diagnostic challenge.
Vahabi SM +6 more
europepmc +2 more sources
A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations
Journal 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 +1 more source
Histological variability and the importance of clinicopathological correlation in cutaneous Rosai-Dorfman disease [PDF]
Anais Brasileiros de Dermatologia, 2016 : Rosai-Dorfman disease is a benign histiocytic proliferative disorder of unknown etiology. The disease mainly affects lymph node tissue, although it is rarely confined to the skin.
Ana Gameiro +3 more
doaj +1 more source
The Clinicopathologic Spectrum of Rosai-Dorfman-Destombes Disease in Adults: An Analysis of 16 Cases. [PDF]
Eur J HaematolABSTRACT 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
New cases expand the genotype, phenotype and therapeutic landscape of H syndrome. [PDF]
Br J HaematolBritish Journal of Haematology, Volume 208, Issue 1, Page 363-366, January 2026.
Triaille C +10 more
europepmc +2 more sources
Sinus Histiocytosis with Massive Lymphadenopathy [PDF]
CA: 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
Rosai‐Dorfman disease in 6‐year‐old child: Presentation, diagnosis, and treatment
Clinical 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
Nodal histiocytic disorder in children: report of three cases and review of literature
The Egyptian Journal of Otolaryngology, 2020 Background Histiocytic system consists of phagocytes and dendritic cells. Both are found in lymph nodes. Usually, this disorder presents with painless cervical lymph node enlargement hence frequently mistaken for lymphoma or tuberculosis.
Indumathi Ainer +3 more
doaj +1 more source