Results 61 to 70 of about 10,817 (231)

Pericardial Effusion and Tamponade as the Manifestation of Erdheim–Chester Disease

Annals of Internal Medicine: Clinical Cases
We hereby report the case of a 77-year-old man hospitalized due to pericardial effusion and tamponade. Upon investigating potential etiologies of the pericardial effusion, we diagnosed him with non-Langerhans cell histiocytosis, also known as Erdheim ...
María Andreo Galera, Daniela D'Urso Soriano, Selene Falcón-Vega, Ana Quiles-Recuenco, Fernando Lidón Pérez, Francisco López García, Félix Gutiérrez Rodero   +6 more
doaj   +1 more source

Indeterminate Cell Histiocytosis in Association with Acute Myeloid Leukemia

Dermatology Research and Practice, 2010
Indeterminate cell histiocytosis (ICH) is a rare proliferative disorder, in which the predominant cells share morphologic and immunophenotypic features from both Langerhans and non-Langerhans cell histiocytosis. We describe a 62-year-old man presenting a
Filipa Ventura, Teresa Pereira, Maria da Luz Duarte, Herlander Marques, Fernando Pardal, Celeste Brito   +5 more
doaj   +1 more source

Langerhans cell histiocytosis of liver

, 2020
Langerhans cell histiocytosis (LCH) is a rare disorder of unknown etiology caused by proliferation of Langerhans cells. It can involve single organ system to multi organ systems and clinical presentation is variable depending on the organ involved and ...
Patodiya, Bharat, Duvuru, Nageshwar Reddy, Samudrala, Swapna, Sekaran, Anuradha   +3 more
core   +1 more source

Chronic Ulcer on the Vulva

JEADV Clinical Practice, EarlyView.
Farhanaz Panjshiri, Reed Gioe, Carole Bitar   +2 more
wiley   +1 more source

Scabies mimicking mastocytosis in two infants

The Turkish Journal of Pediatrics, 2013
Scabies is a common parasitic human infection in infants and children. However, diagnostic pitfalls are frequent in infants, in whom the clinical presentation is usually atypical and different from that in adults.
Emine Cölgeçen-Özel, Ragıp Ertaş, Serap Utaş, Olgun Kontaş   +3 more
doaj  

Erdheim-Chester Disease: Utility of 18F-FDG Positron Emission Tomography [PDF]

Journal of Clinical and Diagnostic Research, 2018
Erdheim-Chester Disease (ECD) is a rare non Langerhans cell histiocytosis of unknown origin with multiorgan involvement. We report a case of a man who presented to us with haematuria, asthenia, fever, nausea and malleolar oedema.
Angelina Cistaro, Maria Licari, Simone Margotti, Daniele Penna, Vincenzo Arena   +4 more
doaj   +1 more source

A Rare Case of Cutaneous Crystal‐Storing Histiocytosis With Kappa Light Chain Restriction and Unusual BCL6 Expression

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Crystal‐storing histiocytosis (CSH) is a rare histopathologic phenomenon characterized by the accumulation of crystalline material within histiocytes, most often associated with lymphoplasmacytic or plasma cell neoplasms. Cutaneous involvement is uncommon and may present diagnostic challenges.
Liangli Wang, Jonathan L. Curry, Julia Dai, Daniel H. Wang, Paolo Strati, Melody R. Becnel, Leomar Y. Ballester, Carlos A. Torres‐Cabala, Phyu P. Aung   +8 more
wiley   +1 more source

A rare cutaneous lesion in the neonatal period: The non-Langerhans cell histiocytosis

Marmara Medical Journal, 2020
The non-Langerhans cell histiocytosis (non-LCH) is a group of diseases characterized by cutaneous involvement in the neonatal period. The non-LCH affects less than 1 in 200,000 children born each year. A definitive diagnosis is important for the treatment of the disease.
Adnan BARUTCU, Ferda OZLU, Hacer YAPICIOGLU YILDIZDAS, Mehmet SATAR   +3 more
openaire   +3 more sources

Langerhans cell histiocytosis of the orbit

, 2013
Purpose: The management of Langerhans cell histiocytosis is controversial.
KIRATLI, HAYYAM, Tarlan, Bercin, Soylemezoglu, Figen   +2 more
core   +1 more source

The 2025 ATS/ERS update of the international multidisciplinary classification of the interstitial pneumonias: implications for the pathologist

Histopathology, EarlyView.
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, Wendy A. Cooper, Aurelie Fabre, William Travis, Lida P. Hariri, Ayodeji Adegunsoye, Sara Piciucchi, Christopher J Ryerson   +7 more
wiley   +1 more source