Results 91 to 100 of about 24,465 (270)

ALK‐Positive Histiocytosis With Unilateral Breast Involvement: A Case Report

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT APH is a rare disorder characterized by the proliferation of ALK‐expressing histiocytes with variable anatomical involvement; however, mammary involvement is exceptionally rare. A 32‐year‐old woman presented with a painless right breast mass. Ultrasound identified a 9 × 8 mm hypoechoic nodule, categorized as BI‐RADS 4A.
Xuechun Liu, Dong Ren, Yanfang Liang
wiley   +1 more source

Langerhans cell histiocytosis presenting as eosinophilic granuloma of the bilateral forearms in an 8-year-old girl: a case report

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, Hind Cherrabi, Boubacar Efared, Kassim Sidibé, Karima Attaraf, Lamiae Chater, Abderahmane Afifi   +6 more
doaj   +1 more source

Periodontal manifestations of Langerhans cell histiocytosis: a systematic review [PDF]

, 2021
Julia C. Difloe‐Geisert, Selina A. Bernauer, Noémie Schneeberger, Michael M. Bornstein, Clemens Walter   +4 more
openalex   +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, Fisher, Max, Kamino, Hideko, Soter, Nicholas A   +3 more
openaire   +4 more sources

Longitudinal Patterns of Fatigue in Long‐Term Survivors of Childhood and Adolescent Cancers: A Report From the Swiss Childhood Cancer Survivor Study

Pediatric Blood &Cancer, Volume 73, Issue 1, January 2026.
ABSTRACT Background Fatigue negatively affects quality of life. We aimed to compare the prevalence of fatigue in survivors of childhood cancer with the Swiss general population, describe longitudinal patterns of fatigue, and identify characteristics associated with persistent fatigue in survivors.
Salome Christen, Luzius Mader, André O. von Bueren, Eva Maria Tinner, Grit Sommer, Christina Schindera, Claudia E. Kuehni, Katharina Roser, Gisela Michel   +8 more
wiley   +1 more source

Polyostotic Langerhans cell histiocytosis presenting as halitosis in a 24-year-old man: a case report

Journal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare disease of the reticuloendothelial system. This report presents a novel case of Langerhans cell histiocytosis with systemic involvement that started with a simple chief complaint.
Hassan Mirmohammad Sadeghi, Sanaz Gholami Toghchi, Fatemeh Mashhadiabbas, Milad Baseri, Maryam Mohammadalizadeh Chafjiri, Parnian Nikraftar, Ardeshir Khorsand   +6 more
doaj   +1 more source

Sotatercept in Pulmonary Langerhans Cell Histiocytosis‐Associated Pulmonary Hypertension: A Case Series and Systematic Review

Pulmonary Circulation, Volume 16, Issue 1, January 2026.
ABSTRACT Pulmonary Langerhans cell histiocytosis (PLCH) frequently complicated by pulmonary hypertension (PH), which markedly worsens prognosis. We retrospectively reviewed three institutional PLCH‐PH cases treated with off‐label Sotatercept added to background triple therapy and performed a systematic review of published PLCH‐PH reports (PubMed/Embase
Giorgi Chilingarashvili, Ruben Joseph Mylvaganam, Roberto J. Bernardo, Aimal Shah, Michael Cuttica, Tara Roberts, Nathaniel Marchetti, Parth Rali   +7 more
wiley   +1 more source

Primary oral manifestation of Langerhans cell histiocytosis refractory to conventional therapy but susceptible to BRAF-specific treatment: a case report and review of the literature [PDF]

, 2019
Langerhans cell histiocytosis (LCH) is a diagnostic and therapeutic challenge. We report on a rare case of its primary oral manifestation that was treated successfully with the BRAF-specific agent, vemurafenib, after insufficient standard LCH treatment ...
Beck-Broichsitter, Benedicta, Doueiri, Mohemed-Salim, Heiland, Max, Lissat, Andrej, Neckel, Norbert, Raguse, Jan-Dirk, Spors, Birgit, Stackelberg, Arendt von, Thieme, Nadine   +8 more
core   +1 more source

The Application of Orthopedic Surgical Robot‐Assisted Technology in Various Clinical Scenarios Involving Bone Tumors

Orthopaedic Surgery, Volume 18, Issue 1, Page 53-65, January 2026.
Robot‐assisted surgery facilitates precise path planning and osteotomy plane identification. With the combination of an orthopedic robot and intraoperative ultrasound or the da Vinci robot, it can enhance the precision and safety of bone tumor surgery. Furthermore, it can be integrated with patient‐specific cutting guides to minimize surgical duration.
Hanxiao Yin, Yiwei Fu, Xirenijiang Yikemu, Weihai Liu, Changye Zou, Xianbiao Xie, Zhiqiang Zhao, Puyi Sheng, Jingnan Shen, Junqiang Yin   +9 more
wiley   +1 more source

Insights into etiology and management of a case of Langerhans cell histiocytosis manifesting as perianal lesions: a case report

Journal of Medical Case Reports
Background 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