Results 161 to 170 of about 100,070 (311)

Recent advances in interstitial lung disease research [PDF]

, 2006
The interstitial lung diseases are a diverse collection of disorders characterized by impaired gas exchange, restricted physiology on lung function testing, and diffuse parenchymal lung infiltrates on radiography.
Vassallo, Robert
core  

Recurrence of recipient Langerhans' cell histiocytosis following bilateral lung transplantation [PDF]

, 1998
Shahid Habib, Johnson Yates Congleton, Denis H. Carr, Judith Partridge, B Corrin, DM Geddes, Nicholas R. Banner, Magdi H. Yacoub, Margaret Burke   +8 more
openalex   +1 more source

Elderly male patient presenting with jaundice and cholangitis brings an unexpected histopathological finding, case report

Heliyon
In this report, we present a case of the first-time manifestation of Langerhans cell histiocytosis in the biliary tract of a 79-year-old male patient. Cholangiocarcinoma was the suspected diagnosis, based on the patient's painless jaundice.
Gergana Nenova, Dietrich A. Ruess, Sophia Chikhladze, Heiko Becker, Sylvia Timme-Bronsert, Uwe Wittel   +5 more
doaj  

Cell mechanics, environmental geometry, and cell polarity control cell-cell collision outcomes [PDF]

arXiv
Interactions between crawling cells, which are essential for many biological processes, can be quantified by measuring cell-cell collisions. Conventionally, experiments of cell-cell collisions are conducted on two-dimensional flat substrates, where colliding cells repolarize and move away upon contact with one another in "contact inhibition of ...
arxiv  

Multisystem Langerhans' cell histiocytosis (Hand-Schüller-Christian disease) in an adult: a case report and review of the literature [PDF]

, 2018
Langerhans' cell histiocytosis (LCH) is a rare and enigmatic clonal disorder that affects mainly children. It is characterized by single or multiple granulomatous mass lesions composed of cells with the Langerhans' cell phenotype.
Jaques, B., Lombardi, T., Monnier, P., Scolozzi, P.   +3 more
core  

Paediatric Langerhans cell histiocytosis with diabetes insipidus: remarkable recovery journey

Journal of the Pakistan Medical Association
A rare condition known as Langerhans cell histiocytosis (LCH) is characterised by the clonal growth of dendritic cells called Langerhans cells, which play a significant role in the immune system. A diverse range of clinical presentations are probable as
Versha Rani Rai, Zulqarnain Buriro, Roshia Parveen, Mohsina Noor, Heeranand Rathore   +4 more
doaj   +1 more source

A neonatal pustule:Langerhans cell histiocytosis [PDF]

, 2019
Langerhans cell histiocytosis (LCH) is a rare, clinically heterogeneous disease that most commonly occurs in pediatric populations. Congenital self-limited LCH is a benign variant of LCH.
Hogeling, Marcia, Kang, Yuna, Knowles, Byron, McKenzie, Shanice, Vecerek, Natalia   +4 more
core  

CT Findings of Orbital Langerhans Cell Histiocytosis [PDF]

, 2000
Gina Yi, Hye Kyung Yoon, Bo Kyung Kim, Kyeong Ah Kim, In Wook Choo   +4 more
openalex   +1 more source

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   +3 more sources

Intestinal Langerhans cell histiocytosis presenting with symptoms similar to inflammatory bowel disease: a case report

Pathology and Oncology Research
Background:Langerhans cell histiocytosis is a rare disease characterized by the abnormal proliferation of Langerhans cells within a single organ or multiple organs.
Yuqing Liu, Zhenwei Chen, Lu Wang, Baizhou Li   +3 more
doaj   +1 more source