Results 91 to 100 of about 4,903,700 (215)
Respirology Case Reports, Volume 14, Issue 9, September 2026.A 50‐year‐old woman presented with recurrent spontaneous pneumothorax and bilateral pulmonary cysts. Whole‐exome sequencing identified a pathogenic FLCN variant, confirming Birt‐Hogg‐Dubé (BHD) syndrome 15 years after symptom onset. This case highlights BHD as an underrecognized cause of diffuse cystic lung disease.
Chia‐Ni Liu +2 more
wiley +1 more source
Immune Checkpoint Inhibitor‐Induced Pancreatitis
United European Gastroenterology Journal, Volume 14, Issue 7, September 2026.ABSTRACT The increasing use of immune checkpoint inhibitors (ICI) has led to recognition of a broad spectrum of treatment‐associated inflammatory adverse events, including pancreatic injury. Histological overlap between ICI associated pancreatic injury (ICIPI) and so‐called autoimmune pancreatitis (AIP) has been suggested in isolated reports, but the ...
Carlos Fernandez Moro +9 more
wiley +1 more source
Multifocal Langerhans Cell Histiocytosis in an Adult
, 2017 Eosinophilic granuloma (EG) is the most common and benign form of the spectrum of disorders referred to as Langerhans cell histiocytosis (LCH). Langerhans cell histiocytosis is primarily regarded as a pediatric disease, with few adult cases of multifocal
Nielsen, Natalie +3 more
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Histopathology, Volume 89, Issue 3, Page 403-425, September 2026.This review highlights changes relevant to pathologists in the updated multidisciplinary classification of interstitial pneumonias. Changes include expansion beyond idiopathic disease, subclassification as interstitial (fibrotic vs non‐fibrotic) and alveolar filling disorders, expansion to include additional patterns (e.g.
Andrew G Nicholson +7 more
wiley +1 more source
Occult Langerhans Cell Histiocytosis in Clear Cell Renal Cell Carcinoma
, 2017 Langerhans cell histiocytosis is a rare disease that is characterized by a localized or systemic proliferation of Langerhans dendritic cells and a wide spectrum of clinical presentations.
Phil Hyun Song, Mi Jin Gu, Hee Jung Kwon
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Endocrine manifestations in Langerhans cell histiocytosis.
, 2007 Langerhans cell histiocytosis is a rare, multisystem disease that shows a particular predilection for hypothalamo-pituitary axis involvement. Diabetes insipidus is the most frequent permanent consequence of Langerhans cell histiocytosis, developing in ...
Chrousos, GP +4 more
core +3 more sources
Journal of Medical Case ReportsBackground 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
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 +6 more
doaj +1 more source
Perifollicular Langerhans cell histiocytosis
Dermatology Online Journal, 2012 A 25-year-old man presented with a 13-year history of an erythematous, papular eruption of his face and trunk, which was treated in the past as acne and psoriasis with isotretinoin and methotrexate, respectively. Histopathologic examination demonstrated an infiltrate of Langerhans cells, which was consistent with Langerhans cell histiocytosis.
Mir, Adnan +3 more
openaire +4 more sources
Cutaneous Langerhans Cell Histiocytosis
, 2008 We report a 4-year-old boy with localized Langerhans cell histiocytosis. The lesions were restricted to the skin of his back, eyelids, glans penis and prepuce for 2 years. Histopathological and electron microscopic examinations showed typical features of
吳亮遠;蔡呈芳;陳佑甫;洪志明 +1 more
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