Results 51 to 60 of about 66,714 (254)
DiagnosticsBackground/Objectives: Lymphedema, a common source of disability among oncology patients, necessitates continuous targeted rehabilitation. Recent studies have revealed the role of connective tissue in this pathology; however, despite existing research on
Carmelo Pirri +6 more
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Idiopathic Calcinosis Cutis over Elbow in a 12-Year Old Child
Case Reports in Orthopedics, 2013 Calcinosis cutis is an uncommon disorder caused by an abnormal deposit of calcium phosphate in the skin in various parts of the body. Four main types of calcinosis cutis have been recognized according to etiology: associated with localized or widespread ...
S. K. Venkatesh Gupta +2 more
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Recalcitrant lymphocytoma cutis successfully treated with mycophenolate mofetil
SAGE Open Medical Case Reports, 2021 Lymphocytoma cutis reflects an exaggerated local immunologic reaction to a stimulus presenting on the head, neck, or upper extremities as a firm 1–3 cm erythematous and/or violaceous plaque or nodule. However, lymphocytoma cutis may be difficult to treat
Farhan Mahmood +2 more
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Clinico-cytomorphological spectrum of calcinosis cutis
Journal of Cytology, 2023 Introduction: The deposition of calcium in the skin is known as calcinosis cutis. It can affect any part of the body and can mimic soft tissue or bony lesions clinically.
Malvika Shastri +4 more
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Histology of non-melanoma skin cancers. An Update [PDF]
, 2017 Non-melanoma skin cancer (NMSC) is the most frequently diagnosed cancer in humans. Several different non-melanoma skin cancers have been reported in the literature, with several histologic variants that frequently cause important differential diagnoses ...
Cantisani, Carmen +4 more
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Aplasia Cutis Congenita as a Sole Manifestation of Congenital Varicella Syndrome
Case Reports in Pediatrics, 2020 Aplasia cutis congenita following maternal varicella is well known. On the other hand, aplasia cutis congenita as the sole manifestation of congenital varicella syndrome is very rare. A perusal of the literature revealed only one case.
Alexander K. C. Leung +2 more
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Novel PLCG2 Mutation in a Patient With APLAID and Cutis Laxa
Frontiers in Immunology, 2018 Background: The auto-inflammation and phospholipase Cγ2 (PLCγ2)-associated antibody deficiency and immune dysregulation (APLAID) syndrome is a rare primary immunodeficiency caused by a gain-of-function mutation S707Y in the PLCG2 gene previously ...
J. Neves +13 more
semanticscholar +1 more source
A case of epigastric heteropagus twinning with other congenital abnormalities in a Chihuahua puppy [PDF]
, 2012 A two-year-old Chihuahua was presented on day 58 of pregnancy due to very marked abdominal distension. A cesarean section was performed and five normal and one clearly abnormal puppy were delivered.
Barrand, KR, Cornillie, Pieter, House, J
core
The Primacy of Ethics in Aesthetic Medicine: A Review
Plastic and Reconstructive Surgery, Global OpenBackground:. The landscape of modern aesthetic medicine has witnessed a paradigm shift from traditional doctor-led care to a consumer-driven model, presenting a plethora of ethical challenges.
Sylvia Ramirez, MD, MPH, MBA +3 more
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Keratoglobus with ARCL1B (EFEMP2 gene) cutis laxa
American Journal of Ophthalmology Case Reports, 2019 Purpose: To report a case of keratoglobus in a patient with autosomal recessive (AR) cutis laxa. Observations: A 38 year old male presented with decreased vision in both eyes uncorrectable with spectacles and a history of corneal rupture in the left eye ...
Thomas F. Mauger +3 more
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