Results 71 to 80 of about 5,248,297 (184)

Langerhans cell histiocytosis: bilateral temporal bone involvement in an adult with diabetes insipidus

B-ENT, 2010
Langerhans cell histiocytosis: bilateral temporal bone involvement in an adult with diabetes insipidus. Objective: To present a clinical case of an adult affected by Langerhans cell histiocytosis with bilateral, nonsimultaneous, involvement of the ...
G. C. Modugno, C. Brandolini, G. Magnani, G. G. Ferri, E. Sabattini, A. Pirodda   +5 more
doaj   +2 more sources

Infantile Central Nervous System Juvenile Xanthogranuloma With Somatic CSF1R Mutation Responsive to Imatinib Monotherapy

Pediatric Blood &Cancer, Volume 73, Issue 10, October 2026.
ABSTRACT Juvenile xanthogranuloma (JXG) of the central nervous system (CNS) is a rare non‐Langerhans cell histiocytosis. CSF1R mutations have been reported for peripheral JXG, but not in CNS JXG. A 3‐month‐old male presented with fever, lymphadenopathy, and macrocephaly with bulging fontanelles.
Sima Vazquez, Kayla Etienne, Long Di, Valerie Martinez‐Torres, Andrew Rosenberg, Sakir H. Gultekin, Aditi Dhir, Bradley Gampel, Heather J. McCrea   +8 more
wiley   +1 more source

Langerhans Cell Histiocytosis (LCH) and Diabetes Insipidus with Mandibular lesion

, 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, Mohammad Reza Mohajeri Tehrani, Bgher Larijani, Somaye Khosravi   +3 more
core  

Pulmonary Langerhans' cell histiocytosis (histiocytosis X) following metastasising malignant melanoma

, 2002
Background: Pulmonary Langerhans' cell histiocytosis (histiocytosis X) is an uncommon, diffuse interstitial lung disease of unknown cause, mostly presenting in young smokers.
Mirzaie, Masoud, Tirilomis, Theodor, Dalichau, H., Zenker, Dieter   +3 more
core   +1 more source

Polyostotic Langerhans cell histiocytosis presenting as halitosis in a 24-year-old man: a case report

Journal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare disease of the reticuloendothelial system. This report presents a novel case of Langerhans cell histiocytosis with systemic involvement that started with a simple chief complaint.
Hassan Mirmohammad Sadeghi, Sanaz Gholami Toghchi, Fatemeh Mashhadiabbas, Milad Baseri, Maryam Mohammadalizadeh Chafjiri, Parnian Nikraftar, Ardeshir Khorsand   +6 more
doaj   +1 more source

An Overlap of Erdheim–Chester Disease and Rosai–Dorfman Disease With Isolated Bone Lesions Presenting a Diagnostic Challenge: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Some of the rarest diseases with cell accumulation in different organs are histiocytoses. Since these diagnoses are uncommon, other differential diagnoses must be excluded. We report a case of a 42‐year‐old man with episodes of knee pain and fever.
Maris Tulk, Reet Kuuse, Maksim Zagura, Hazem M. M. Ali, Liis Vahesaar   +4 more
wiley   +1 more source

[Unusual pulmonary presentation of systemic Langerhans cell histiocytosis]

, 2008
An 80-year-old nonsmoking man was referred to our hospital with bilateral perihilar pulmonary opacities. He had a history of epilepsy, sclerosing cholangitis, cutaneous lesions previously diagnosed as localised Langerhans cell histiocytosis.
Schuller, A, Lega, J-C, Schuller, Aurélien, Lazor, R, Lega, Jean-Christophe, Cottin, Vincent, Cordier, J F, Cordier, Jean-François, Jullien, D, Lazor, Romain, Jullien, Denis, Cottin, V   +11 more
core   +1 more source

Spontaneous resolution of unifocal Langerhans cell histiocytosis of the skull : potential role of ultrasound in detection and imaging follow-up [PDF]

, 2018
Langerhans cell histiocytosis is a tumor-like condition characterized by idiopathic proliferation of Langerhans cells. The disease may involve the skeleton as well as other organs systems. Bone involvement may be solitary or multifocal.
Verlooy, Joris, Mania De Praeter, Filip M. Vanhoenacker, Vanhoenacker, Filip, Joris Verlooy, Vanhoenacker, Filip M., De Praeter, Mania   +6 more
core   +1 more source

Langerhans cell histiocytosis: A rare cause of pathological rib fracture

, 2021
Langerhans cell histiocytosis, formerly known as histiocytosis X, represents clonal proliferations of the antigen-presenting dendritic cells, which are normally found in many organs. It is a rare disease which tends to affect children and adolescents. In
Yolcu A., Temiz P., Aydoğdu İ., Tulay C.M., Tulay, Cumhur Murat, Yolcu, Alkım, TEMİZ, PEYKER, Aydoğdu, İsmet   +7 more
core   +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