Results 51 to 60 of about 31,021 (191)

Efficacy of vinblastine in central nervous system Langerhans cell histiocytosis: a nationwide retrospective study [PDF]

open access: yes, 2011
Background Vinblastine (VBL) is the standard treatment for systemic Langerhans cell histiocytosis (LCH), but little is known about its efficacy in central nervous system (CNS) mass lesions. Methods
Sophie Ng Wing Tin   +30 more
core   +2 more sources

Canal Cholesteatoma Presentation and Management: A Systematic Review and Meta‐Analysis

open access: yesOtolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective To evaluate current understanding of external auditory canal cholesteatoma (EACC), its symptomatic burden, clinical features, diagnostic approach, and management strategies to reduce delays in diagnosis. Data Sources PubMed, CINAHL, COCHRANE Library, and SCOPUS.
Angelica M. Walker   +6 more
wiley   +1 more source

Splenic sea-blue (ceroid) histiocytosis due to hypertriglyceridemia: Report of a case and review of literature

open access: yesHuman Pathology: Case Reports, 2017
Sea-blue histiocytosis is a rare condition that can be often identified in bone marrow, spleen, liver as well as other organs. It can be frequently detected in bone marrow of patients with myeloproliferative neoplasms as well as non-neoplastic conditions
Kacy A. Krehbiel   +3 more
doaj   +1 more source

Clinical characteristics and survival of children with Langerhans cell hystiocytosis [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2008
INTRODUCTION Langerhans cell histiocytosis is a rare disease in children, initial presentation is variable, clinical course, prognosis and survival are mostly unpredictable.
Krstovski Nada   +3 more
doaj   +1 more source

Genetic analysis of primary lung interdigitating dendritic cell sarcomas

open access: yesThe Journal of Pathology, EarlyView.
Abstract Interdigitating dendritic cell sarcomas (IDCSs) are rare tumors that commonly arise in the hematopoietic system and rarely outside. The genetic drivers of IDCS carcinogenesis are unknown; therefore, therapeutic options are limited. We investigated somatic gene mutations and copy‐number alterations (CNAs) in nine IDCSs arising in the lung by ...
Mikhail S Ermakov   +6 more
wiley   +1 more source

Langerhans cell histiocytosis present in a 1-day-old girl: a case report

open access: yesJournal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare condition characterized by diverse clinical manifestations, ranging from cutaneous lesions to systemic involvement.
Yang Meng
doaj   +1 more source

Cutaneous horn: A rare subtype of juvenile xanthogranuloma

open access: yesClinical Case Reports, 2020
Because of variability in the JXG shape and the extensive range of a cutaneous horn differential diagnosis, dermatologists should keep this diagnosis in their mind in the time of encountering with infants or children cases of cutaneous horn.
Fariba Iraji   +2 more
doaj   +1 more source

CD1a-positive dendritic cell-enriched pigmented purpuric dermatosis in association with dyslipidemia

open access: yesJournal of Dermatology and Dermatologic Surgery, 2022
Indeterminate cells (ICs) are dendritic cells (DCs) that share the histologic features of Langerhans cells and macrophages but lack Birbeck granules. It remains unclear whether IC histiocytosis is a separate disease entity or a reactive process.
Tiffany Hinojosa   +3 more
doaj   +1 more source

Cutaneous Crystal‐Storing Histiocytosis With Marginal Zone Lymphoma. A Case Report With A Striking Clinical Presentation

open access: yesJournal of Cutaneous Pathology, EarlyView.
ABSTRACT Cutaneous crystal‐storing histiocytosis (CSH) is an extremely rare histopathologic finding of histiocytes accumulating crystals of immunoglobulin or paraproteins, often associated with lymphoplasmacytic malignancies. It commonly presents in a wide age range of both female and male adults with a history of a lymphoproliferative disorder ...
Ashton Arlen   +3 more
wiley   +1 more source

CASES OF DISSEMINATED AND GIANT JUVENILE XANTHOGRANULOMA IN CHILDREN

open access: yesПедиатрическая фармакология, 2014
Juvenile xanthogranuloma is the most common clinical variant of the class II histiocytosis. This article presents two clinical observationsof papulonodular juvenile xanthogranuloma, specification of epidemiological data, clinical and histological ...
E. I. Pil'gui   +5 more
doaj   +1 more source

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