Results 161 to 170 of about 64,916 (281)

Case Report: Invasive pulmonary aspergillosis caused by <i>Aspergillus lentulus</i> in a boy with chronic granulomatous disease. [PDF]

Front Med (Lausanne)
Tan S, Liao Q, Wen Y, Zhu Y.
europepmc   +1 more source

Giant cellulitis‐like Sweet's syndrome induced by gilteritinib

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Juan de Luque‐Fernández, Irene Rivera‐Ruiz, Irene Suárez‐Vergne, Inmaculada Sánchez‐Ramírez, Manuel Galán‐Gutiérrez, Antonio José Vélez García‐Nieto   +5 more
wiley   +1 more source

Ulceronecrotic Plaques, Patchy Scalp Alopecia and Visual Disturbance in a 46‐Year‐Old Man

International Journal of Dermatology, EarlyView.
ABSTRACT A 46‐year‐old incarcerated man with chronic hepatitis C infection and intravenous drug use presented with a rapidly progressive pruritic eruption involving the scalp, trunk, and limbs, accompanied by patchy scalp alopecia and bilateral panuveitis.
Alex Majri, Austen Anderson, Jeremy Ng, Nima Mesbah‐Ardakani   +3 more
wiley   +1 more source

Rhinoscleroma Masquerading as a Nasal Mass: A Diagnostic Challenge in a Young Adult. [PDF]

Cureus
Pandharmise R, Harkare V, Khadakkar SP, Idrees FI, Dholkawala SD.   +4 more
europepmc   +1 more source

Olaparib‐associated cutaneous vasculitis in a patient with breast cancer

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Marcial Álvarez‐Salafranca, Teresa Puértolas, Adrián Diago, María Carmen Gómez‐Mateo   +3 more
wiley   +1 more source

Australian clinical practice guideline: diagnosis and treatment of idiopathic multicentric Castleman disease

Internal Medicine Journal, EarlyView.
Abstract Idiopathic multicentric Castleman disease (iMCD) is a rare condition. The pathogenesis is incompletely understood; however, interleukin‐6 (IL‐6) is a major mediator. The clinical presentation is heterogeneous, from mild constitutional symptoms to severe multi‐organ failure.
Dipti Talaulikar, Jun Yen Ng, Adam Bryant, Annmarie Bosco, Hugh C. Caterson, Pratyush Giri, Pravin Hissaria, Simon J. Harrison, Stephen Lade, Connull Leslie, Jacinta Perram, H. Miles Prince, Dejan Radeski, Maureen Rischmueller, Craig Wallington‐Gates, Nicholas Weber, Alberta Hoi   +16 more
wiley   +1 more source

Cutaneous Alternariosis

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Kaan Yilmaz, Viola Pflüger, Cyrill Géraud   +2 more
wiley   +1 more source

When to consider an inborn error of immunity: clues for physicians

Internal Medicine Journal, EarlyView.
Abstract The term inborn errors of immunity (IEIs) refers to the rapidly expanding group of genetic disorders causing dysregulation of the immune system. With improved genetic testing in recent years, the number of defined IEIs and their range of phenotypic presentations has grown vastly, with more than 550 IEIs now described.
Meera Thangarajah, Lucinda J. Berglund
wiley   +1 more source

Tuberculous/BCG-Related Chronic Orchiepididymitis With Fistulization: Expanded Case Report and Literature Review. [PDF]

Case Rep Urol
Bernardo G, Carvalho JA, Alzamora M, Lobo J, Morais A.   +4 more
europepmc   +1 more source

Anthracofibrosis: an under‐recognised mimic of malignancy and tuberculosis in a migrant population

Internal Medicine Journal, EarlyView.
Abstract Anthracosis, usually regarded as a benign and uncommon bronchoscopic finding, was identified in 108 (9.9%) of 1154 bronchoscopy procedures at two Australian hospitals, with almost a third showing bronchial narrowing consistent with anthracofibrosis.
Wai Yiu, Paul T. King, Martin I. MacDonald   +2 more
wiley   +1 more source