Results 11 to 20 of about 1,612 (168)

Letterer–Siwe Disease (LSD): A Case Report [PDF]

Sudan Journal of Medical Sciences, 2018
Background: Letterer–Siwe Disease (LSD) is one of the variants of Langerhans cell histiocytosis (LCH), which is considered as a rare disease that affects many systems in the body; it is characterized by monoclonal migration and proliferation of specific ...
Suad H. H., Mona Mohamed Elamin, Gad Allah Modawe, Khalid Abd Elmohsin Awad Elseed   +3 more
doaj   +2 more sources

Enfermedad de Letterer-Siwe: diagnóstico dermatológico de una enfermedad sistémica [PDF]

Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica, 2019
Se presenta el caso de una paciente de 8 meses de edad, con masa en el mediastino, lesiones líticas en sacabocado en la radiografía de cráneo, pápulas y máculas violáceas en palmas y pliegue infraumbilical y leve esplenomegalia.
María Cristina Trujillo, Paulina Uribe, María Isabel Arredondo, Ana Cristina Ruiz   +3 more
doaj   +1 more source

Congenital self-healing reticulohistiocytosis: An atypical presentation acquired in a 10-month-old. [PDF]

Clin Case Rep, 2022
Congenital self‐healing reticulohistiocytosis (CSHR) presents at birth; however, in this case, it is acquired at 10 months of age which is atypical. CSHR is benign and it must be differentiated from malignant form of Langerhans Cell Histiocytosis. Abstract Congenital self‐healing reticulohistiocytosis of Hashimoto and Pritzker (CSHR) is a rare, benign ...
Yuki CS, Young PJ, Ohsie S, Nguyen X.
europepmc   +2 more sources

LETTERER-SIWE'S DISEASE

American Journal of Diseases of Children, 1936
In reviewing the literature in an attempt to identify the condition in the case which we are here reporting, we have found that Letterer,1in 1924 under the title "Aleukamische Retikulose (Ein Beitrag zu den proliferativen Erkrankungen des Retikuloendothelialapparates)," described the occurrence of splenohepatomegaly, associated with anemia, and a ...
ARTHUR F. ABT, EDWARD J. DENENHOLZ
core   +4 more sources

Recognising cutaneous tuberculosis. [PDF]

J Dtsch Dermatol Ges
Summary Tuberculosis (TB) continues to be a leading cause of death in many countries, and also remains a significant concern in Germany, particularly due to migration. The diagnosis of rare cutaneous tuberculosis is challenging as it manifests in various clinical forms that resemble more common dermatological conditions.
Gramminger C, Biedermann T.
europepmc   +2 more sources

Letterer-Siwe disease presenting with gastrointestinal and cutaneous manifestations [PDF]

, 2023
Histiocytosis is a set of distinct proliferative illnesses defined by the proliferation and infiltration of varied numbers of dendritic cells, macrophages, and monocytes in the afflicted tissues.
Tamrazova, Olga Borisovna, Zakharova, Irina Nikolaevna, Pristanskova, Ekaterina Andreevna, Skobeev, Dmitry Alexandrovich, Abbas, Walaa Fadhil, Stadnikova, Antonina Sergeevna, Berezhnaya, Irina Vladimirovna, Goncharova, Lyudmila Viktorovna   +7 more
core   +1 more source

Langerhans cell histiocytosis in a pediatric patient: A typical presentation with oral manifestations

Clinical Case Reports, Volume 11, Issue 7, July 2023., 2023
Key Clinical Message Langerhans cell histiocytosis (LCH) is a rare hematological disorder characterized by abnormal proliferation of Langerhans cells. Head and neck region is commonly involved with oral manifestations appearing first in many instances. A thorough knowledge of the disorder and an interdisciplinary approach warrant for the better outcome
Royasa Shakya, Bandana Koirala, Ashok Dongol, Iccha Kumar Maharjan, Shashi Keshwar, Neetu Jain, Ashish Shrestha   +6 more
wiley   +1 more source

Successful treatment of orbital Langerhans cell histiocytosis with stereotactic radiosurgery: A case report and literature review

Clinical Case Reports, Volume 11, Issue 6, June 2023., 2023
MRI of the brain demonstrating Langerhans Cell Histiocytosis (LCH) of an orbit. Key Clinical Message Langerhans cell histiocytosis (LCH) is a rare inflammatory myeloid neoplasm arising from the proliferation of pathologic Langerhans cells. LCH has a spectrum of presentations predominantly affecting male pediatric patients.
Emily Etter, Benjamin Bosse, Yi Peng Wang, Susan Hiniker, Justin Oh   +4 more
wiley   +1 more source

A case report of adult Langerhans cell histiocytosis and review of the literature

Clinical Case Reports, Volume 11, Issue 2, February 2023., 2023
Oral LCH is rare, its first manifestations are mostly oral and its prognosis in early stages is good but if it progresses its's fatal; therefore, it is important that dentists are aware of this disease, its different clinical manifestations, and patient management.
Fatemeh Lavaee, Ali Dehghani Nazhvani, Aylar Afshari   +2 more
wiley   +1 more source

Anti‐inflammatory, Antinociceptive, and Toxicological Properties of Uvaria comperei Stem Crude Extract and Fractions

BioMed Research International, Volume 2023, Issue 1, 2023., 2023
The present study was carried out to investigate the anti‐inflammatory activity of a methanolic extract and fractions of Uvaria comperei stems. The crude extract was obtained by maceration of the powder in methanol and fractions by vacuum chromatography from the methanolic extract.
Marguerite Kamdem Simo, Gael Tchokomeni Siwe, Maurice Taboula Kayo, Zheng Chen, Mersimine Mangoua Kouamo, Darline Dize, Pierre Dongmo Jazet, Modeste Lambert Sameza, Fabrice Boyom Fekam, Guglielmina Froldi, Muhammad Muddassir Ali   +10 more
wiley   +1 more source