Results 91 to 100 of about 5,248,297 (184)

Cystic Lung Changes in Inclusion Body Myositis: An Unusual Pulmonary Manifestation

Respirology Case Reports, Volume 14, Issue 10, October 2026.
This report highlights a rare case of inclusion body myositis presenting with pulmonary disease. ABSTRACT Idiopathic inflammatory myopathies (IIMs) are chronic autoimmune disorders affecting skeletal muscles, with pulmonary involvement in 30%–40% of cases. Inclusion body myositis (IBM) is a distinct subset that usually does not involve the lungs.
Gehad Othman, Thasniya Ummer, Heshani De Silva, Harshana Bandara, Hector Chinoy   +4 more
wiley   +1 more source

Langerhans cell histiocytosis in monocygote twins: case reports.

, 1996
Langerhans cell histiocytosis includes three clinical forms of histiocytosis X. We describe a disseminated form of Langerhans cell histiocytosis (Letterer-Siwe disease) in monozygotic twins.
Mader I, Stock KW, Steinbrich W, Radue EW   +3 more
core   +1 more source

Langerhans cell histiocytosis presenting as eosinophilic granuloma of the bilateral forearms in an 8-year-old girl: a case report

Journal of Medical Case Reports, 2019
Background Langerhans cell histiocytosis previously known as histiocytosis X is a rare disease of children and young adults with a very broad clinical spectrum. In children, its annual incidence is estimated between 0.2–0.5 per 100,000.
Salahoudine Idrissa, Hind Cherrabi, Boubacar Efared, Kassim Sidibé, Karima Attaraf, Lamiae Chater, Abderahmane Afifi   +6 more
doaj   +1 more source

Hypermanganesemia in Children With Liver and Portosystemic Circulation Disorders: A Systematic Review

Journal of Paediatrics and Child Health, Volume 62, Issue 10, Page 1848-1858, October 2026.
ABSTRACT Aim Children with chronic liver disease and portosystemic circulation disorders may have long‐term neurocognitive problems. Hypermanganesemia, reported in this group, could be a contributor. This systematic review aimed to characterise liver and portosystemic circulation disorders associated with hypermanganesemia and reported neurocognitive ...
Helena J. Kim, Susan M. Siew, Ji Hyun Moon, Tracey A. Williams, S. Murthy Chennapragada, Gordon Thomas, Shekeeb S. Mohammad   +6 more
wiley   +1 more source

Insights into etiology and management of a case of Langerhans cell histiocytosis manifesting as perianal lesions: a case report

Journal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare disorder characterized by abnormal proliferation of Langerhans cells, primarily affecting children and occasionally adults.
Pei Xiao-yue, Tai Zixin, Zhang Wen-jun
doaj   +1 more source

Pulmonary Langerhans Cell Histiocytosis

, 2010
Pulmonary Langerhans cell histiocytosis is an uncommon interstitial lung disease that results from the accumulation of cells known as Langerhans cells in the lung. It primarily affects young smokers. High resolution chest computed tomography findings are
Furtun K., Salih Bilgin, Burcin Celik, Kamil Furtun, Bilgin S., Çelik B.   +5 more
core   +1 more source

Langerhans Cell Histiocytosis (Letterer-Siwe disease ) - Report of a case

, 2011
Langerhans cell histiocytosis is a rare disorder that occurs when there aretoo many of type of white blood cell called a Langerhans cell. We describe a3-months infant girl who developed wide spread skin lesions since she was 4days of age. . The diagnosis
BS Elagraa, Elagraa, BS, El Hassan, AM, MA Abdulla, SI Ayed, Ayed, SI, Abdulla, MA, AM El Hassan   +7 more
core   +1 more source

Langerhans Cell Histiocytosis: Single Center Experience of 25 Years

, 2019
Objectives: To review a single center outcome of patients with Langerhans Cell Histiocytosis diagnosed at a tertiary referral hospital from ...
Kurugoglu, S., Adaletli, I, Celkan, T., Tuysuz, G., Yildiz, I, Apak, H., Bozkurt, S., Ozdemir, N., Dervisoglu, S., Apak, Hilmi, Kurugoglu, Sebuh   +10 more
core   +1 more source

Systemic findings of Langerhans cell histiocytosis in neonatal period

Revista de la Facultad de Ciencias de la Salud, 2011
We report an unusual case of mediastinal abcessed mass, with involvement of the lung, thymus and probably bone and hematopoietic system, in a newborn that was diagnosed with Langerhans cell histiocytosis.
Rosalba Días-Castro, Gloria Martínez, Claudia Elena Cruz, Ivonne Meza, Germán Ruiz, Alex Ortíz, Donaldo Pasaje   +6 more
doaj   +2 more sources

Bilateral choroidal osteoma associated with langerhans cell histiocytosis, a coincidence?

, 2019
Purpose: To describe a case of bilateral choroidal osteoma (CO) in a patient with a history of langerhans cell histiocytosis (LCH). Methods: A 24-year-old man complaining of gradually decreasing visual acuity in both eyes is presented.
Negar Aliabadi, Mohammd Riazi Esfahani, Fariba Ghassemi, Alireza Khodabande, Pejvak Azadi   +4 more
core   +1 more source