Results 51 to 60 of about 111,579 (167)

Sinus and palatal Rosai-Dorfman Disease: Case report and review of the literature

American Journal of Otolaryngology
Rosai-Dorfman Disease (RDD) is a rare non-Langerhans cell histiocytosis. We present a unique case of RDD with sinus and palatal involvement managed with surgical biopsy, debulking and radiation, and review the literature on this topic.
Clare Moffatt, Hanna K. Mandl, Jessa E. Miller, Jonathan W. Said, Elliot Abemayor, Daniel M. Beswick   +5 more
doaj   +1 more source

Rosai-Dorfman Disease- A Surprise diagnosis in Follow up of SCC Pyriform Sinus -Post Surgery and CTRT [PDF]

National Journal of Laboratory Medicine, 2013
Rosai-Dorfman disease also known as Sinus Histiocytosis with massive Lymphadenopathy (SHML). SHML was first described by Rosai and Dorfman in 1969 [1] and is now considered a non malignant inflammatory disorder in which the precise origin of ...
Nandeesh M, Anitha T.K., Santosh R.
doaj   +1 more source

Multidisciplinary Exploration of Computed‐Tomographic and Ancient‐DNA Data of an Iron Age Skull From Latvia With Multiple Lytic Bone Lesions: Differential Diagnosis Between Metastatic Carcinoma, Multiple Myeloma and Skeletal Tuberculosis

Ecology and Evolution, Volume 16, Issue 7, July 2026.
In this study we used a combined computed tomographic and archaeogenetic approach to analyse a skull and vertebra with lytic lesions from a disturbed grave in the Čunkāni‐Dreņģeri cemetery in Latvia, dated to 10th century CE. Both methodologies were used to evaluate a proposed differential diagnosis of multiple myeloma, metastatic carcinoma and bone ...
Alise Akermane‐Pokšāne, Jānis Ķimsis, Elīna Pētersone‐Gordina, Antonija Vilcāne, Guntis Gerhards, Mārtiņš Pēterfelds, Renāte Ranka   +6 more
wiley   +1 more source

A case of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) in a patient with diffuse large B-cell lymphoma and chronic hepatitis B virus infection

Терапевтический архив, 2012
The paper describes a case of diffuse large B-cell lymphoma detected in a patient 13 months after sinus histiocytosis with massive lymphadenopathy (SHML) or Rosai-Dorfman disease (RDD) being diagnosed together with active hepatitis B virus infection ...
A L Melikian, A M Kovrigina, E A Giliazitdinova, M K Gitis   +3 more
doaj  

Next‐Generation Paleopathology: Using Commercial AI in Bioarchaeological Diagnosis

International Journal of Osteoarchaeology, Volume 36, Issue 4, Page 844-858, July/August 2026.
ABSTRACT Artificial intelligence encompasses computational systems capable of performing cognitive functions such as learning, reasoning, and problem‐solving. Within this domain, generative AI and large language models such as ChatGPT, Gemini, and Copilot have shown significant potential in clinical diagnostics.
Jessica Mongillo, Giulia Vescovo, Giulia Manzo, Nicoletta Zedda, Barbara Bramanti   +4 more
wiley   +1 more source

Rosai-Dorfman Disease: Self-Resolving Unilateral Lymphadenopathy and a Brief Review of Literature

Case Reports in Oncological Medicine, 2018
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy (SHML), is a disease of histiocytic proliferation with no known pathogenesis.
Joshua Feriante, Richard T. Lee
doaj   +1 more source

Case for diagnosis [PDF]

Anais Brasileiros de Dermatologia, 2014
Cutaneous Rosai-Dorfman disease is a rare, lymphoproliferative disease. It is benign and self-limited, only involves skin and subcutaneous tissue and typically occurs as histiocyte-rich inflammatory infiltrates, manifesting as erythematous to brown ...
Han Ma, Huaiqiu Huang, Meirong Li, Wei Lai, Chun Lu   +4 more
doaj   +1 more source

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) and oligoarthritis

, 2011
A 24-year-old woman who had sinus histiocytosis with massive lymphadenopathy (SHML, Rosai-Dorfman disease) also had oligoarthritis. We found only four previously reported cases of SHML with clinical joint disease.
Alexander-Kaï So, Anca Mihaescu, So, A.K., Julien Castioni, Castioni, J., Mihaescu, A.   +5 more
core   +1 more source

Skull Base Langerhans Cell Histiocytosis with Diabetes Insipidus and Panhypopituitarism- A Rare Clinical Entity

Bengal Journal of Otolaryngology and Head Neck Surgery, 2017
Introduction A case of Langerhans cell histiocytosis (LGH) involving extensive area of base of skull resulting in panhypopituitarism and diabetes insipidus (DI) is reported.
Anirban Ghosh, Mithun Chaudhury, Abhishek Mukherjee   +2 more
doaj   +3 more sources

Homonymous Superior Quadrantanopia due to Erdheim-Chester Disease with Asymptomatic Pituitary Involvement

Case Reports in Neurological Medicine, 2017
Polyostotic sclerosing histiocytosis, also known as Erdheim-Chester disease (ECD), is a rare form of non-Langerhans histiocytosis. ECD has wide clinical spectrums which mainly affect skeletal, neurological, dermatological, retroperitoneal, cardiac, and ...
Roaa Ridha Amer, Sara Mohammed Qubaiban, Eman Abdulkarim Bakhsh   +2 more
doaj   +1 more source