Results 71 to 80 of about 5,230,024 (304)
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 +5 more
wiley +1 more source
Disseminated histiocytoses biomarkers beyond BRAFV600E: frequent expression of PD-L1. [PDF]
, 2015 The histiocytoses are rare tumors characterized by the primary accumulation and tissue infiltration of histiocytes and dendritic cells. Identification of the activating BRAFV600E mutation in Erdheim-Chester disease (ECD) and Langerhans cell histiocytosis
Arceci, Robert J +8 more
core +3 more sources
Journal of Cutaneous Pathology, Volume 52, Issue 9, Page 554-567, September 2025.ABSTRACT Langerhans cell sarcoma (LCS) is a rare neoplastic proliferation of Langerhans cell with aggressive clinical behavior and involves multiple organ systems, including the skin. LCS is characterized by marked cytologic atypia, frequent mitoses including atypical ones, and expression of CD1a, S100, and langerin (CD207).
Randa Obid +8 more
wiley +1 more source
Pulmonary langerhans cell granulomatosis (histiocytosis X)
Туберкулез и болезни лёгких, 2014 Pulmonary Langerhans cell granulomatosis is a rare disease. Its causes are unknown and accurate data on its prevalence are lacking. This disease is characterized by the formation of lung tissue granulomas consisting of activated Langerhans cells ...
A. A. Sadovnikov, K. I. Panchenko
doaj
Diagnostic problems and surgical treatment of histiocytosis X [PDF]
Medicinski Glasnik, 2007 A 16-year-old boy, with swelling and pain in the left submandibular region was treated at the Clinic for Maxillofacial Surgery. The x-ray examination showed destructive bone lesion of the mandibulae left side and oval lesions on the left hand bone and ...
Alkhalil M, A. Redžić, A. Smajilagić
doaj
Secondary aneurysmal bone cyst in Langerhans cell histiocytosis: Case report, literature review
European Journal of Radiology Open, 2019 Langerhans cell histiocytosis (LCH) is a rare disease of the myeloid precursor cells, it predominantly occurs in the skull and long bones as unifocal bone lesions. Aneurysmal bone cysts (ABC) are benign, expansive and lytic bone. Reports of secondary ABC
P. Lomoro +6 more
doaj +1 more source
Treatment of Xanthoma disseminatum – a systematic literature review
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 9, Page 1061-1069, September 2025.Summary Xanthoma disseminatum is a rare disease from the spectrum of non‐Langerhans cell histiocytoses, which can be categorized into three types and is sometimes associated with systemic involvement. Due to the its rarity, there are no standardized treatment guidelines for this disease, making treatment in everyday clinical practice more difficult ...
Inga Hansen‐Abeck +4 more
wiley +1 more source
Langerhans Cell Histiocytosis (LCH) and Diabetes Insipidus with Mandibular lesion
Electronic Physician, 2012 Langerhans cell histicytosis (LCH) is a rare disorder that primarily affects children. Its occurrence in adult is very rare. We report a case of 42 year old female patient who presented polyuria and polydipsia, loosing teeth and diplopia added to symptom
Sayeh Alizad jahani +3 more
doaj
Histiocitosis de células de Langerhans en el raquis infantil [PDF]
, 2006 Introducción: la Histiocitosis de células de Langerhans incluye un amplio espectro de enfermedades de etiología desconocida, observada preponderantemente en niños.
Fernández, Claudio A. +2 more
core
High viral load of Merkel cell polyomavirus DNA sequences in Langerhans cell sarcoma tissues. [PDF]
, 2014 International audienceBACKGROUND: Langerhans cell (LC) sarcoma (LCS) is a high-grade neoplasm with overtly malignant cytologic features and an LC phenotype.
A Kanik +38 more
core +4 more sources