Results 121 to 130 of about 79,497 (273)

Mycosis Fungoides in Paediatric Patients: A Real‐Life Retrospective Study

JEADV Clinical Practice, EarlyView.
Our study represents the largest cohort of children with MF worldwide, providing relevant evidence supporting phototherapy as first‐line treatment, with an overall remission rate of 36.36%. Both topical and systemic therapy also showed favourable outcomes.
Mariana de la Vega, María Antonieta Domínguez Gómez, Martha Alejandra Morales‐Sánchez   +2 more
wiley   +1 more source

Chronic Granulomatous Disease [PDF]

Nature, 1987
Curnutte Jt, Babior Bm
openaire   +6 more sources

Strawberry Gingivitis and Septal Perforation as Onset Manifestations of Granulomatosis With Polyangiitis Triggered by COVID‐19

JEADV Clinical Practice, EarlyView.
ABSTRACT Strawberry gingivitis is a rare but characteristic manifestation of granulomatosis with polyangiitis (GPA), characterized by red‐purple, swollen, granular gingiva. We report a 31‐year‐old woman who developed GPA following a mild COVID‐19 infection, presenting with fever, fatigue, facial pain, chronic sinusitis, epistaxis and strawberry ...
A. Segarra‐Ponce, Lucero Itsaí Quintana‐Romero, María José Zorrilla‐Marina, Bertha Lissette Sotelo‐García, Marisol Ramírez‐Padilla   +4 more
wiley   +1 more source

Cutaneous Manifestations in Inflammatory Bowel Diseases [PDF]

, 2015
Inflammatory bowel diseases have a high frequency in Europe. They are chronic disorders that evolve with relapses and remissions. Clinical features include the signs of underlying inflammatory bowel disease and also signs of extraintestinal ...
Benea, Vasile, Costescu, Monica, Georgescu, Simona Roxana, Mitran, Cristina Iulia, Mitran, Madalina Irina, Sarbu, Maria Isabela, Tampa, Mircea   +6 more
core   +2 more sources

Ulcerative C2 neurocutaneous dysesthesia (trigeminal trophic syndrome in an alternative distribution) [PDF]

, 2020
Trigeminal trophic syndrome is an uncommon condition characterized by paresthesia, itch, and self-inflicted wounds following the trigeminal dermatome(s). Similar processes adhering to cervical nerve distributions have been reported, calling into question
Hajar, Tamar, Haynes, Dylan, Keller, Jesse J, Ortega-Loayza, Alex G, Topham, Christina, White, Kevin P   +5 more
core  

COLLAB: A Global Survey of Clinical and Laboratory Assessment in Alopecia Areata by Hair Specialists

JEADV Clinical Practice, EarlyView.
ABSTRACT Background Alopecia areata (AA) is a common non‐scarring alopecia. Data continue to emerge on associations with autoimmune and other conditions. Janus kinase inhibitors (JAKi) are increasingly used to treat AA. Objectives The aim was to assess variation in laboratory testing in patients with AA among hair experts internationally and to compare
Cathal O'Connor, Aoife Boyle, Leila Asfour, Bevin Bhoyrul, Laita Bokhari, George Cotsarelis, Chantal Cotter, Brittany Craiglow, Lara Cutlar, Rachita Dhurat, Ncoza Dlova, Isabella Doche, Jeff Donovan, Aaron M. Drucker, Samantha Eisman, Daniel Fernandes Melo, Matthew J. Harries, Maria Hordinsky, Ahmed Kazmi, Brett King, Antonios Kolios, Nekma Meah, Paradi Mirmirani, Arash Mostaghimi, Manabu Ohyama, Yuliya Ovcharenko, Rodrigo Pirmez, Bianca Maria Piraccini, Lidia Rudnicka, David Saceda‐Corralo, Jerry Shapiro, Cathryn Sibbald, Rod Sinclair, Blake R. C. Smith, Michela Starace, Sergio Vaño‐Galván, Wei Liang Koh, Katherine York, Ian McDonald, Dmitri Wall   +39 more
wiley   +1 more source

Cutaneous Vasculitis as a Covid‐19 Manifestation: A Cross‐Sectional Study With Detailed Histopathological Evaluation

JEADV Clinical Practice, EarlyView.
Multiple cutaneous manifestations have been linked with COVID‐19, including cutaneous vasculitis, ranging from mild or asymptomatic to fulminant. We conducted a comprehensive study investigating the cutaneous and histopathological manifestations of vasculitis in 33 patients with COVID‐19.
Reem Diab, Azadeh Rakhshan, Mohammad Shahidi Dadras, Sareh Salarinejad, Ali Kaddah, Zahra Razzaghi, Marwa Akhdar, Roxanna Sadoughifar, Fahimeh Abdollahimajd   +8 more
wiley   +1 more source

RESPIRATORY MANIFESTATIONS OF CHRONIC GRANULOMATOUS DISEASE; A CLINICAL SURVEY OF PATIENTS FROM IRANIAN PRIMARY IMMUNODEFICIENCY REGISTRY

Iranian Journal of Allergy, Asthma and Immunology, 2003
Chronic granulomatous disease represents a group of inherited disorders of phagocytic system wherein recurrent infections are seen at different sites especially in the respiratory system.
M. Movahedi, A. Aghamohammadi, A. Farhondi, M. Moin, Zahra Pourpak, M. Gharagozlou, D. Mansoiiri, A. Babaei Jandaghi, N. Shahnavaz, N. Rezaei, K. Abolmaali, Sh. Alizadeh Arasi, J. Bakhshaei, M. Vaziri   +13 more
doaj  

The Rare Presentation of Deep Dermatophytosis‐Trichophyton in an Immunosuppressed Patient

JEADV Clinical Practice, EarlyView.
ABSTRACT Dermatophytes typically cause superficial skin infections characterized by an active border. However, they can present atypically invading deeper in immunocompromised patients. We present a case of a 72‐year‐old woman with bullous pemphigoid who had received oral prednisolone for 3 months and developed umbilicated papules.
Jidapa Triwatcharikorn, Nitina Yeesibsean, Jirapon Jesrichai, Chanat Kumtornrut   +3 more
wiley   +1 more source

BCGiosis as a presenting feature of a child with chronic granulomatous disease

Brazilian Journal of Infectious Diseases
Bacillus Calmette Guerin (BCG) vaccine, which is administered to all newborns in some regions, could lead to serious complication ranging from local disease (known as BCGitis) to disseminated disease (BCGosis) in a group of patients with primary ...
Zahra Movahedi, Sayna Norouzi, Setareh Mamishi, Nima Rezaei   +3 more
doaj   +1 more source