Results 21 to 30 of about 903 (178)

Clinical Images: Spotted bone: Incidental detection of a rare genetic disease. [PDF]

open access: yesACR Open Rheumatol, 2022
ACR Open Rheumatology, Volume 4, Issue 3, Page 221-222, March 2022.
Ramirez DA, Bettendorf B.
europepmc   +2 more sources

Linear Focal Elastosis: A Peculiar Dermatosis. [PDF]

open access: yesClin Case Rep
LFE confirmed by orcein stain showing fragmented elastic fibers within the reticular dermis. ABSTRACT Linear focal elastosis (LFE), also known as elastotic striae, is a rare cutaneous condition characterized by abnormal or increased deposition of elastic fibers in the dermis.
Ahmad A   +3 more
europepmc   +2 more sources

A Case of Skin Lesion in a Child and Radiological Lesions in His Father

open access: yesJEADV Clinical Practice
JEADV Clinical Practice, Volume 4, Issue 2, Page 630-632, June 2025.
Jeanne Renuy   +4 more
doaj   +2 more sources

Imaging Features of Mandibular Ramus Osteoma on Computed Tomography: A Case Report With Literature Analysis. [PDF]

open access: yesCase Rep Dent
Osteomas are benign, mesenchymal, and slow‐growing lesions that arise from the surface of the bone and consist primarily of lamellar/cortical‐type bone. They are characterized by the proliferation of compact or cancellous bone. The most common locations for osteoma to originate are the mandible and paranasal sinuses.
Gattuso E, Casto AL, Cumbo EMG.
europepmc   +2 more sources

osteopoikilosis and fracture healing: the bone quantity-quality paradox-a case report and systematic review with synthesis without meta-analysis. [PDF]

open access: yesOrthop Rev (Pavia)
Introduction Osteopoikilosis is a rare sclerosing bone dysplasia that may mimic osteoblastic metastases and complicate fracture assessment.
Suwanaratana R   +2 more
europepmc   +2 more sources

Connective Tissue Naevus

open access: yesIndian Journal of Dermatology, 1999
A young adult female patient of connective tissue naevus presented with papules and indurated plaques on both les and left arm. Histopathology showed increased amount of collagen in the dermis. Osteopoikilosis was absent.
Bhat Ramesh M   +2 more
doaj   +1 more source

Osteopoiquilosis: reporte de un caso y revisión bibliográfica Osteopoikilosis: Report of a case and review of the current literature

open access: yesActa Médica Costarricense, 2012
Paciente masculino de diecinueve años de edad, proveniente de Guápiles, con antecedente de tortículis congénita y urolitiasis obstructiva a repetición, con un cuadro clínico de varios meses de evolución de dolor en miembros inferiores, fue referido por ...
José Carlos Alonso-Escalante   +2 more
doaj   +1 more source

Osteopoikilosis: A Cause of Elevated Bone Mineral Density on Dual X-Ray Absorptiometry Measurement in a Young Woman: Case Report

open access: yesTürk Osteoporoz Dergisi, 2010
Osteopoikilosis (OPK) is an asymptomatic, rare bone dysplasia. It causes an increase in bone density. The etiology and pathogenesis is unknown. OPK is generally diagnosed incidentally on plain radiographies which were performed for other locomotor system
Asylbek Kaparov   +3 more
doaj   +2 more sources

Increased Bone Formation and Accelerated Bone Mass Accrual in a Man Presenting with Diffuse Osteosclerosis/High Bone Mass Phenotype and Adenocarcinoma of Unknown Primary

open access: yesJBMR Plus, Volume 7, Issue 8, August 2023., 2023
Lumbar spine and femoral neck BMD showed marked increases in the 18 months prior to presentation with incidental osteosclerosis. Iliac crest biopsy reveals dense trabecular bone reflecting sclerosis at the time of presentation. ABSTRACT A 71‐year‐old man was referred for evaluation of incidental generalized osteosclerosis.
Terrence H. Diamond   +6 more
wiley   +1 more source

Poliartraljinin Nadir Bir Sebebi: Osteopoikilozis

open access: yesSakarya Tıp Dergisi, 2021
Osteopoikilosis or spotted bone disease is a rare bone dysplasia of unknown etiology. It is characterized by an abnormality in bone maturation process and often found incidentally on radiologic examination.
Özlem Altındağ   +3 more
doaj   +1 more source

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