Results 71 to 80 of about 14,916 (217)

Treatment of Xanthoma disseminatum – a systematic literature review

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 9, Page 1061-1069, September 2025.
Summary Xanthoma disseminatum is a rare disease from the spectrum of non‐Langerhans cell histiocytoses, which can be categorized into three types and is sometimes associated with systemic involvement. Due to the its rarity, there are no standardized treatment guidelines for this disease, making treatment in everyday clinical practice more difficult ...
Inga Hansen‐Abeck, Mina Hillemans, Finn Abeck, Stefan W. Schneider, Nina Booken   +4 more
wiley   +1 more source

CASE OF GUILLAIN-BARRE´ SYNDROME IN A PATIENT WITH PULMONARY LANGERHANS CELL HYSTIOCYTOSIS

Архивъ внутренней медицины, 2019
Langerhans cell histiocytosis is a rare disease characterized by various clinical patterns: from isolated lung lesions to severe involvement of other organs.
E. V. Efremova, A. V. Vasil’chev, A. M. Shutov, A. S. Podusov, I. Yu Troshina, A. A. Timofeev   +5 more
doaj   +1 more source

Late-Onset Langerhans Cell Histiocytosis Presenting with Seizures and Bilateral Temporal Involvement

Archives of Epilepsy, 2022
Langerhans cell histiocytosis is known as a rare childhood disease. In this case, we wanted to share our patient’s experience whose first symptom was an epileptic seizure, which attracted attention at an advanced age and revealed bilateral temporal lobe ...
Özge Öcek, Hasan Kuş, Pınar Ortan
doaj   +1 more source

Therapie des Xanthoma disseminatum – eine systematische Literaturrecherche

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 9, Page 1061-1070, September 2025.
Zusammenfassung Das Xanthoma disseminatum ist eine seltene Erkrankung aus dem Spektrum der Nicht‐Langerhans‐Zell‐Histiozytosen, welche in drei Gruppen eingeteilt werden kann und teilweise mit einer Systembeteiligung einhergeht. Da die Erkrankung selten ist, fehlen standardisierte Therapierichtlinien, wodurch die Behandlung im klinischen Alltag ...
Inga Hansen‐Abeck, Mina Hillemans, Finn Abeck, Stefan W. Schneider, Nina Booken   +4 more
wiley   +1 more source

Novel report of an osteogenic tumor in a late Jurassic Mamenchisaurid from Thailand

Journal of Anatomy, Volume 247, Issue 3-4, Page 699-711, September/October 2025.
Here we describe a pathology in an ulna of a Late Jurassic mamenchisaurid from Thailand. We use anatomical descriptions, CT scanning, and bone histology to identify the pathology as an osteogenic tumor. Abstract Here we report on an osseous abnormality and multiple fractures in an ulna of a subadult basal Eusauropod (Mamenchisauridae) from the Late ...
Siripat Kaikaew, Suravech Suteethorn, Anusuya Chinsamy   +2 more
wiley   +1 more source

Involving Adolescents in Decision‐Making in Pediatric Organ Transplantation: A Qualitative Study in Switzerland

Pediatric Transplantation, Volume 29, Issue 6, September 2025.
This is the first interview study exploring the perspectives of transplanted adolescents on decision‐making regarding transplantation, and it shows that they want to be part of decision‐making at different levels of involvement. ABSTRACT Background In pediatrics, the triadic relationships between the adolescent, parents, and healthcare providers, as ...
Alana Vallo‐Sacchettini, Cristina Zimmermann, Olivier Janjic, Michael Rost, Bernice Elger   +4 more
wiley   +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

Doença de células de langerhans e mama.

Acta Médica Portuguesa, 2011
Langerhans cell histiocytosis (LCH) is a rare systemic disorder, with a diversified presentation and natural history. It can compromise any organ. We report a case of a 32-year-old woman who came to our clinic with an asymptomatic palpable breast mass ...
Cátia Rodrigues, Paulo Santos, Dora Simões, Maria Odete Valério, C Calhaz-Jorge   +4 more
doaj   +1 more source

Class 3 MAPK Mutation in Langerhans cell histiocytosis and Trametinib—Reporting Two Contrarian Responses

Pediatric Blood &Cancer, Volume 72, Issue 10, October 2025.
Natalia Wojciechowska, Alejandra Cervantes‐Dominguez, Jason Wang, Anish Ray   +3 more
wiley   +1 more source

Adverse Physical Health Outcomes and Healthcare Service Utilization in Siblings of Children With Cancer: A Systematic Review

Cancer Medicine, Volume 14, Issue 15, August 2025.
ABSTRACT Introduction Siblings of children with cancer may be vulnerable to compromised long‐term health. We aimed to describe the frequency (prevalence, incidence) of adverse physical health outcomes and healthcare service utilization among siblings of children with cancer and compare the risk of the above outcomes to siblings of children without ...
Victorine Sirveaux, Lily Puterman‐Salzman, Yue Qian Zhang, Eleni Sotirakos, Philippe Dodin, Guillaume Dumas, Eyal Cohen, Nadia Roumeliotis, Petros Pechlivanoglou, Hallie Coltin   +9 more
wiley   +1 more source