Results 41 to 50 of about 1,752 (171)
Clinical Case Reports, Volume 12, Issue 6, June 2024.Key Clinical Message Intracranial RDD is rare medical event mimicking different diagnoses. Although the surgical resection is the best treatment option, but radiation therapy can also achieves long‐term suboptimal outcomes. Abstract An 83‐year‐old male with a history of tension‐type headaches was evaluated.
Hamid Nasrollahi +6 more
wiley +1 more source
Sinus histiocytosis with massive lymphadenopathy [PDF]
, 2019 Two cases of a recently described entity, 'sinus histiocytosis with massive lymphadenopathy,' occurring in Black males, are reported. Prominent cervical adenopathy was the main presenting feature in both. Histologically, these nodes were characterised by
Kahn, L.B. +2 more
core +1 more source
International Consensus Statement on Allergy and Rhinology: Sinonasal Tumors
International Forum of Allergy &Rhinology, Volume 14, Issue 2, Page 149-608, February 2024.Abstract Background Sinonasal neoplasms, whether benign and malignant, pose a significant challenge to clinicians and represent a model area for multidisciplinary collaboration in order to optimize patient care. The International Consensus Statement on Allergy and Rhinology: Sinonasal Tumors (ICSNT) aims to summarize the best available evidence and ...
Edward C. Kuan +158 more
wiley +1 more source
Journal of Cutaneous Pathology, Volume 51, Issue 1, Page 7-10, January 2024.Abstract Rosai–Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy (SHML), is a rare subtype of reactive histiocytosis which is seldom associated with Hodgkin's and non‐Hodgkin's lymphomas. To date, the coexistence in the same patient of extra nodal SHML and primary cutaneous B‐cell lymphoma (PCBCL) has been reported in the ...
Gabriele Roccuzzo +8 more
wiley +1 more source
Extra-osseous involvement of Langerhans' cell histiocytosis in children [PDF]
, 2018 The predominant clinical and radiological features of Langerhans' cell histiocytosis (LCH) in children are due to osseous involvement. Extra-osseous disease is far less common, occurring in association with bone disease or in isolation; nearly all ...
Eich, Georg +5 more
core
A Case of Rosai‐Dorfman Disease Successfully Treated by Corticotherapy
Case Reports in Hematology, Volume 2024, Issue 1, 2024.Rosai‐Dorfman disease (RDD) is a benign histiocytic proliferation that results in nodal and extranodal involvements. It is a rare disease, with fewer than 1,000 cases reported in the literature, which explains its lack of knowledge by physicians and the lack of codified therapeutic strategies.
Alioune Badara Diallo +8 more
wiley +1 more source
Paranasal Rosai-Dorfman Disease with Osseous Destruction [PDF]
, 2017 Rosai-Dorfman disease is a rare histiocytic proliferative disorder of unknown etiology typically characterized by cervical lymphadenopathy. Extranodal involvement often manifests in the head and neck region. We present a 10-year-old male who presented to
Changxing Liu +2 more
core +2 more sources
Sinus histiocytosis with massive lymphadenopathy : is the lymph node enlargement always massive? [PDF]
, 2007 Sinus histiocytosis with massive lymphadenopathy (SHML) is a benign proliferating histiocytic disorder, predominantly of lymph nodes with extra-nodal involvement in some cases.
Jain, Shyama +2 more
core
Extranodal (cutaneous) Rosai Dorfman: a rare presentation [PDF]
, 2017 Rosai Dorfman disease is a rare histiocytic disorder of unknown etiology commonly involving the cervical lymph nodes first described in 1969, Extranodal involvement is very rare.
Ghodake, Nishant, Khadatkar, Ashwini
core +2 more sources
, 2018 Rosai-Dorfman disease is a rare, usually benign, entity that mostly affects children and adolescents. We report a clinical case in which the most common clinical and imaging manifestation is present: cervical lymphadenopathy. Histological confirmation is
Carvalho, André +5 more
core +2 more sources