Results 51 to 60 of about 3,839 (216)

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease): Report of a case in a Nigerian Teaching Hospital

Nigerian Dental Journal, 2011
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare, benign disease of unknown aetiology. This disease typically presents with massive, painless cervical lymphadenopathy but may occur in a wide variety of extranodal sites.
O. F. Ajayi, O. A. Effiom, W. L. Adeyemo, O. M. Gbotolorun, W. Akinshipo   +4 more
doaj   +1 more source

Childhood Cancer Survivors in Latin America: Insights Into Health Outcomes and Information Needs

Pediatric Blood &Cancer, Volume 72, Issue 9, September 2025.
ABSTRACT Background Childhood cancer survivors (CCSs) face long‐term health challenges, yet the health and specific needs of Latin American survivors remain underexplored. This study aimed to describe the health‐related, psychosocial late effects, and information needs among CCSs in the region. Methods This mixed‐method study combined quantitative data
Ana Carolina Izurieta‐Pacheco, David H. Noyd, Julia Challinor, Nuria Rossell, Maria Fernanda Olarte‐Sierra, Daniel Bastardo Blanco, Marcela Zubieta, Nicholas B. George, Sara Perez‐Jaume, Anna Felip‐Badia, Viviana Trigoso, Patricia Loggetto, Valeska Gonzalez, Carlos Frias, Sinders Rincon, Roberta Ortiz, Soad Fuentes‐Alabi de Aparicio, Liliana Vásquez Ponce   +17 more
wiley   +1 more source

HLA‐DR+ CD8+ T lymphocytes as an alternative T‐cell activation marker in pediatric HLH: A real‐life study

Pediatric Allergy and Immunology, Volume 37, Issue 1, January 2026.
Clément Triaille, Isabel Fernandez, Fabien Touzot   +2 more
wiley   +1 more source

Suspected calcitriol‐mediated hypercalcaemia and postmortem diagnosis of histiocytic sarcoma in a dog

Veterinary Record Case Reports, Volume 13, Issue 3, September 2025.
Abstract This report describes a case of refractory ionised hypercalcaemia, of 12 months duration, in an 11‐year‐old, male, neutered beagle diagnosed with metastatic histiocytic sarcoma at postmortem examination. In this case, the parathyroid hormone levels were at the lower end of the reference interval, the parathyroid hormone‐related peptide was ...
Kerry E. Rolph, Mollie McBride, Gilda Rawlins‐Vaughan, Sarah Cavanaugh, Regina Tose Kemper, Pompei Bolfa   +5 more
wiley   +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

Langerhans cell histiocytosis of the sphenoid sinus: a case report

The Turkish Journal of Pediatrics, 2010
Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is a rare disorder characterized by clonal proliferation and excess accumulation of pathologic Langerhans cells causing local or systemic effects.
Guohua Yu, Fei Huang, Lingling Kong, Xiangmei Kong, Luping Zhang, Qing Xu   +5 more
doaj  

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

Combination of Photodynamic and Bronchoscopic Intervention With Radiation Therapy in Treating Pulmonary Pleomorphic Sarcoma: A Case Report

The Clinical Respiratory Journal, Volume 19, Issue 9, September 2025.
We discuss a case where an innovative combination of photodynamic therapy (PDT) and local radiation therapy to address the diagnostic and therapeutic challenges associated with PPSS resulted in significant improvements in clinical symptoms and patient survival, demonstrating the success of this treatment.
Ran An, Shishou Wang, Lijian Tang, Tao Feng, Chen Lin, Chongqing Lv   +5 more
wiley   +1 more source

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

Steroid‐responsive generalised sterile necrotising pyogranulomatous lymphadenitis in a cat

Journal of Small Animal Practice, Volume 66, Issue 9, Page 670-675, September 2025.
A 1.5‐year‐old neutered male cat was presented with fever, inappetence, lethargy and marked generalised lymphadenopathy of 4 days duration. Excisional biopsy of peripheral lymph nodes revealed necrotising pyogranulomatous lymphadenitis. Extensive investigation failed to identify an underlying infectious [bacterial (Bartonella, Mycobacteria, Mycoplasma,
L. Lecot, E. Ramery, M. Hugonnard, A. Tortereau, É. Krafft   +4 more
wiley   +1 more source