Results 41 to 50 of about 7,686 (174)
International Journal of Cancer, Volume 158, Issue 10, Page 2674-2683, 15 May 2026.What's new? Mitogen‐activated protein kinase (MAPK) inhibitors are promising treatments for pediatric Langerhans cell histiocytosis (LCH), a rare heterogeneous neoplasm that often affects multiple organ systems. Which MAPK inhibitors are most effective against LCH remains uncertain.
Xue Tang +5 more
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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
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Histiocytosis X: Langerhans’ Cell Histiocytosis
Hematology/Oncology Clinics of North America, 1987 Histiocytosis X is a complex and poorly understood entity. Nevertheless, it would appear as if certain themes are found recurrently throughout the literature dealing with this disease and a review of them serves as a useful summary. 1. Problems with Nomenclature.
openaire +2 more sources
The clinicopathological characteristics and differential diagnosis of histiocytosis
Chinese Journal of Contemporary Neurology and Neurosurgery, 2015 The histiocytosis is divided into Langerhans' cell histiocytosis (histiocytosis X) and non-Langerhans' cell histiocytosis (NLCH). The former mainly occurs in lymphatic hematopoietic tissue and often involves central nervous system (CNS).
Shi-zhu YU
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The FASEB Journal, Volume 40, Issue 8, 30 April 2026.Serum SERPINA3 levels were higher in BOS compared to non‐BOS patients. OPG and SERPINA3 positive cells colocalized with tryptase positive mast cells in airways from BOS lung tissue. OPG and SERPINA3 staining positively correlated in partially and completely obstructed airways.
Yanzhe Liu +8 more
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Letterer–Siwe Disease (LSD): A Case Report
Sudan Journal of Medical Sciences, 2018 Background: Letterer–Siwe Disease (LSD) is one of the variants of Langerhans cell histiocytosis (LCH), which is considered as a rare disease that affects many systems in the body; it is characterized by monoclonal migration and proliferation of specific ...
Suad H. H. +3 more
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A CASE OF HISTIOCYTOSIS IN THE PATIENT SUSPECTED TO HAVE PULMONARY TUBERCULOSIS
Туберкулез и болезни лёгких, 2019 The article describes the clinical case of Langerhans cell histiocytosis with lesions in lungs and flat bones in a 40-year-old smoker. During 4 years, all stages of the disease were followed.
M. A. Karnaushkina +2 more
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Pulmonary Circulation, Volume 16, Issue 2, April 2026.ABSTRACT Pulmonary arterial hypertension (PAH) in India is a substantial yet under‐recognized contributor to cardiovascular morbidity and mortality. Its progressive course, nonspecific early manifestations, and heterogeneous aetiologies often lead to delayed diagnosis and fragmented care.
Prashant Bobhate +16 more
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LCH-Histiocytosis from Langerhans Cells in Craniofacial Region
Česká Stomatologie a Praktické Zubní Lékařství, 2005 The authors retrospectively analyze the occurrence of histiocytosis from Langerhans cells (LCH) in a group of patients from the Children Stomatological Clinic in Prague - Motol from the years 1998-2003.
M. Hubáček, J. Kozák
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Langerhans cell histiocytosis in children: a case report and brief review of the literature
PAMJ Clinical Medicine, 2019 Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, is a non-malignant disease involving clonal proliferation of Langerhans cells. It is an orphan disease affecting mainly the child and the young adult.
Zakaria El Ouali +7 more
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