Results 91 to 100 of about 1,275,517 (295)

Isolated anal tuberculosis presenting as an anal fistula in an immunocompetent child

JPGN Reports, EarlyView.
Abstract Extra‐pulmonary tuberculosis accounts for less than 15% of all tuberculosis cases, while intestinal tuberculosis accounts for less than 1% of extra‐pulmonary forms of the disease. Abdominal organ involvement is more common, but extension to the ano‐perineal region is extremely rare.
Mariam Lagrine, Rabiy Elqadiry, Houda Nassih, Aicha Bourrahouat, Imane Ait Sab   +4 more
wiley   +1 more source

Undiagnosed Chronic Granulomatous Disease, Burkholderia cepacia complex Pneumonia, and Acquired Hemophagocytic Lymphohistiocytosis: A Deadly Association

Case Reports in Pulmonology, 2013
Background. Chronic granulomatous disease is a rare inherited disorder of the phagocyte nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. The clinical course of the disease is marked by recurrent infections, including Burkholderia cepacia ...
Maxime Maignan, Colin Verdant, Guillaume F. Bouvet, Michael Van Spall, Yves Berthiaume   +4 more
doaj   +1 more source

Ruxolitinib and vedolizumab salvage therapy in the setting of cytomegalovirus colitis for a patient with newly diagnosed very early onset inflammatory bowel disease

JPGN Reports, EarlyView.
Abstract Acute severe ulcerative colitis increases the risk for cytomegalovirus (CMV) infection, particularly with the use of immunocompromising medications. We report a case of a 4‐year‐old with newly diagnosed very early onset inflammatory bowel disease presenting with acute severe colitis refractory to both corticosteroids and infliximab, whose ...
Alison Laxer, Morris Edelman, Julie Gallagher, Benjamin Sahn   +3 more
wiley   +1 more source

Cutaneous Granulomas Associated With Rubella Replication in TAP Deficiency Syndrome: A Fatal Case Report Evolving Into Cutaneous Squamous Cell Carcinoma and EBV‐Associated Lymphoproliferative Syndrome

JEADV Clinical Practice, EarlyView.
ABSTRACT Transporter associated with antigen presentation (TAP) deficiency syndrome (TDS) is a rare primary immunodeficiency (PID) characterised by a broad spectrum of clinical manifestations, with noninfectious cutaneous granulomas (CG) being a common feature.
A. Fernández‐Galván, M. Aparicio, P. Muñoz, J. Fulgencio‐Barbarín, N. D. Zurita, D. Arroyo‐Sánchez, O. Cabrera‐Marante, L. M. Allende, M. Llamas‐Velasco   +8 more
wiley   +1 more source

Lentiviral gene therapy for X-linked chronic granulomatous disease

Nature Network Boston, 2020
D. Kohn, C. Booth, E. Kang, S. Pai, K. Shaw, G. Santilli, M. Armant, K. Buckland, U. Choi, S. de Ravin, M. Dorsey, C. Kuo, D. León‐Rico, C. Rivat, N. Izotova, K. Gilmour, Katie Snell, Jinhua Xu-Bayford Dip, Jinan Darwish, E. Morris, Dayna Terrazas, Leo D. Wang, C. Bauser, T. Paprotka, D. Kuhns, J. Gregg, H. Raymond, J. Everett, G. Honnet, L. Biasco, P. Newburger, F. Bushman, M. Grez, H. Gaspar, David A. Williams, H. Malech, A. Galy, A. Thrasher, Karen F. Christopher A. Geraldine Manuel H. Bobby Anne A Buckland Bauser Honnet Grez Gaspar Galy Thrasher, K. Buckland, C. Bauser, A. Thrasher   +41 more
semanticscholar   +1 more source

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

Chronic Granulomatous Disease [PDF]

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

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

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

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