Results 201 to 210 of about 47,429 (322)

Prenatal Diagnosis of Proteus Syndrome: About a Case

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.
ABSTRACT Proteus syndrome (PS) is a rare disorder (< 1/1000000), marked by progressive overgrowth commonly impacting the skeleton, skin, adipose tissue, and central nervous system. Clinical criteria were established in 2019. PS arises from a somatic activating variation in the AKT1 gene.
Luana Giovannangeli   +10 more
wiley   +1 more source

Unusual Presentation of Facial Comedones

open access: yesClinical Case Reports, Volume 13, Issue 5, May 2025.
Comedonal lupus is a rare variant of chronic cutaneous lupus erythematosus. Its misleading clinical appearance may delay diagnosis, which relies on histopathology and direct immunofluorescence. Early treatment is essential to prevent scarring. ABSTRACT Not all facial comedonal lesions represent acne, nor are they always benign.
Lamis Elyamani   +2 more
wiley   +1 more source

Basal Cell Nevus Syndrome and Sporadic Basal Cell Carcinoma: A Comparative Study of Clinicopathological Features. [PDF]

open access: yesActa Derm Venereol
Wang CY   +12 more
europepmc   +1 more source

Posttraumatic Epidermoid Inclusion Cyst Following Untreated Orbital‐Zygomaticomaxillary Fracture: Case Report

open access: yesClinical Case Reports, Volume 13, Issue 5, May 2025.
ABSTRACT Timely and comprehensive treatment of craniofacial injuries is essential, as complications may arise, including epidermoid inclusion cysts. We hereby present a case of an orbital epidermoid cyst that developed a year after a patient was involved in a motor vehicle accident and sustained facial injuries that remained untreated.
David Kiwango Deoglas   +2 more
wiley   +1 more source

A Rare Case of Budd–Chiari Syndrome in a Young Female

open access: yesClinical Case Reports, Volume 13, Issue 5, May 2025.
ABSTRACT Budd–Chiari syndrome is a rare disorder characterized by hepatic vein obstruction, with an incidence of 1 in 100,000. It can be diagnosed through imaging studies and initially managed with anticoagulants. Acute Budd–Chiari syndrome can be treated with thrombolysis to dissolve blood clots obstructing hepatic veins.
Joshua Chacko   +5 more
wiley   +1 more source

Congenital Melanocytic Nevus with Neurocristic Cutaneous Hamartoma: A Case Report. [PDF]

open access: yesDermatopathology (Basel)
El-Rayes D   +5 more
europepmc   +1 more source

Recurrent Malignant Melanoma on the Tongue: A Case Report and Review of the Literature

open access: yesCancer Reports, Volume 8, Issue 5, May 2025.
ABSTRACT Background Melanoma of the oral mucosa is an uncommon cancer arising from the tissues lining the mouth. Among oronasal malignant melanomas, tongue melanoma makes up a mere 2%. Optimal treatments for this rare and often late‐stage disease remain elusive.
Maziar Motiee‐Langroudi   +2 more
wiley   +1 more source

Fluorescence <i>in situ</i> hybridization in melanoma diagnosis: Pros and cons. [PDF]

open access: yesExp Ther Med
Mihulecea CJ   +4 more
europepmc   +1 more source

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