Results 51 to 60 of about 4,504 (202)
Localized Langerhans cell histiocytosis masquerading as Brodie s abscess in a 2-year-old child: a case report [PDF]
, 2016 Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, refers to a spectrum of diseases characterized by idiopathic proliferation of histiocytes that produce either focal (localized LCH) or systemic manifestations (Hand–Schüller ...
Chang, Wei-Fang +4 more
core +1 more source
Osteoid Osteoma of the Occipital Condyle in Adolescents: Surgical Resection Under Navigation
Clinical Case Reports, Volume 13, Issue 5, May 2025.ABSTRACT This article reports a 12‐year‐old male with occipital condyle osteoid osteoma, presenting with neck pain and limited motion, unresponsive to conservative treatment. CT revealed a right condylar lesion. Surgical excision via a right paramedian suboccipital incision achieved complete recovery, confirmed by pathology and 3‐month follow‐up.
Yiji Li +8 more
wiley +1 more source
Journal of the Belgian Society of Radiology, 2013 Background: A 51-year-old male was referred to the hospital with pain on the right side of the thorax, without any apparent trauma. There was no medical history. He had a nonproductive cough and smoked 15 cigarettes a day.
BJ Schouten, HM Suliman
doaj +1 more source
Journal of Orthopaedic Reports, 2023 Introduction: Premature puberty, café-au-lait pigmentation, polyostotic fibrous dysplasia, and/or varied endocrine disorders make up the unusual condition known as McCune Albright Syndrome.
Mrinal Mahadev Kambli +5 more
doaj +1 more source
Denosumab treatment for fibrous dysplasia [PDF]
, 2012 Fibrous dysplasia (FD) is a skeletal disease caused by somatic activating mutations of the cyclic adenosine monophosphate (cAMP)‐regulating protein, α‐subunit of the Gs stimulatory protein (G s α).
Albright +41 more
core +1 more source
Post‐COVID‐19 Exacerbation of a Stable Fibrous Dysplasia: A Case Report
Clinical Case Reports, Volume 13, Issue 4, April 2025.ABSTRACT Fibrous dysplasia (FD) is a rare, benign fibro‐osseous lesion characterized by replacement of normal bone with extensive fibrous stroma due to abnormalities in osteoblast differentiation. After puberty and during adulthood, FD lesions usually become quiescent. However, some cases show signs of regrowth and reactivation.
Mohammed Taib Fatih +7 more
wiley +1 more source
Growth of children with Langerhans cell histiocytosis [PDF]
, 1995 Conclusion: GH deficiency is not a common manifestation of LCH in childhood and GH provocation tests are only indicated when there is a poor or decelerating growth rate.
Egeler, R.M. (Maarten) +3 more
core +1 more source
Skeletal Phenotype in Mulibrey Nanism, A Monogenic Skeletal Dysplasia With Fibrous Dysplasia
Clinical Genetics, Volume 107, Issue 3, Page 271-277, March 2025.We present a cross‐sectional detailed radiographic evaluation of the skeletal phenotype in 33 patients, aged 4.5–48 years, with Mulibrey nanism (MUL). This study confirms MUL as a skeletal dysplasia with prenatal‐onset growth failure, slender bones, vertebral changes, and a high prevalence of fibrous dysplasia and fractures.
Susann Karlberg +3 more
wiley +1 more source
Craniofacial polyostotic fibrous dysplasia
Contemporary Clinical Dentistry, 2010 An unusual case of fibrous dysplasia involving right craniofacial region in a female is reported. The clinical features, radiological findings, and treatment have been discussed.
Yadavalli Guruprasad, Chandan Prabhakar
doaj +1 more source
Gorham–Stout disease: good results of bisphosphonate treatment in 6 of 7 patients
Acta Orthopaedica, 2020 Background and purpose — Gorham–Stout disease (GSD) is a rare mono- or polyostotic condition characterized by idiopathic intraosseous proliferation of angiomatous structures resulting in progressive destruction and resorption of bone.
Kristian Nikolaus Schneider +8 more
doaj +1 more source