Results 61 to 70 of about 6,263,315 (249)

Case Reports A case of chronic granulomatous disease

open access: yes, 2014
(Key words: Chronic granulomatous disease; phagocyte ...
S Sriranganathan   +3 more
core  

Pulmonary Aspergillosis in a Previously Healthy 13-Year-Old Boy

open access: yesCanadian Respiratory Journal, 2016
Chronic granulomatous disease (CGD) is a rare, polygenic primary immunodeficiency. In this case report, we describe a previously healthy 13-year-old boy who presented with multifocal pulmonary aspergillosis and was subsequently diagnosed with an ...
Jonathan H. Rayment, Indra Narang
doaj   +1 more source

Therapeutic Challenges in Managing Coexisting Hidradenitis Suppurativa and Squamous Cell Carcinoma: A Clinical Case Study

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Hidradenitis suppurativa (HS) is a chronic inflammatory skin disorder affecting intertriginous areas. Long‐standing HS can undergo malignant transformation into squamous cell carcinoma (SCC), particularly in the perineal and gluteal regions. We report a 54‐year‐old man with severe, treatment‐refractory HS complicated by an aggressive verrucous
Michael Zolotas   +6 more
wiley   +1 more source

Cutaneous Rosai‐Dorfman Disease With MAP2K1 Mutation Treated With Encorafenib and Binimetinib

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Rosai‐Dorfman disease (RDD) is a rare histiocytic disorder with unifocal to multisystemic involvement. Activating mutations in the MAPK/ERK pathway can occur in up to 50% of RDD cases. We report a case of cutaneous RDD (C‐RDD) with facial and truncal lesions harboring an activating MAP2K1 (MEK1) mutation that showed a complete response to a ...
Melike Ak   +2 more
wiley   +1 more source

Colitis as the Sole Initial Presentation of Chronic Granulomatous Disease: Histopathologic Clues to Diagnosis.

open access: yes, 2016
Chronic granulomatous disease is a rare, inherited immunodeficiency disorder that reduces the superoxide generation ability of phagocytes, leading to recurrent infections and granulomatous inflammation.
Vuppula, Sharon   +5 more
core   +1 more source

Surgical Reconstruction of Ulcers in Chronic Granulomatous Disease

open access: yesPlastic and Reconstructive Surgery, Global Open
Summary:. Chronic granulomatous disease can affect multiple organ systems and is associated with poor wound healing, which may preclude a patient from undergoing a bone marrow transplant.
Lucas A. Dvoracek, MD   +4 more
doaj   +1 more source

Eczema‐Like Amelanotic Melanoma: A Diagnostic Challenge

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Amelanotic melanoma (AM) is a rare and aggressive variant of cutaneous melanoma characterised by the absence of pigmentation, often leading to delayed diagnosis due to its ability to mimic benign inflammatory or neoplastic conditions. We report the case of a 68‐year‐old woman presenting with a slowly enlarging, erythematous, mildly scaling ...
Agata Janowska   +8 more
wiley   +1 more source

Schistosoma mansoni in mice: modulation of granulomatous response after reinfection and chemotherapeutic treatment

open access: yesRevista da Sociedade Brasileira de Medicina Tropical, 1994
Mice previously infected with Schistosoma mansoni, and cured by specific treatment (400mg/kg oxamniquine, p. o.) in the chronic phase of the disease, were reinfected 20 days after treatment to assess their capacityfor modulation ofthe granulomatous ...
Paulo Marcos Z. Coelho   +3 more
doaj   +1 more source

Chronic granulomatous disease; Three different clinical presentation [PDF]

open access: yes, 2017
Chronic granulomatous disease is an inherited disorder of nicotinamide-adenine dinucleotide phosphate oxidase and results in a defect in intracellular killing of ingested microorganisms characterized by recurrent life threatening bacterial and fungal ...
Ceyhan, Meltem   +5 more
core   +1 more source

Pericardial effusions in two boys with chronic granulomatous disease. [PDF]

open access: yes, 1999
Pediatr Radiol. 1999 Nov;29(11):820-2. Pericardial effusions in two boys with chronic granulomatous disease. Macedo F, McHugh K, Goldblatt D. SourceDepartment of Radiology, Hospital Geral de Santo Antonio, Porto, Portugal.
MCHUGH, K., MACEDO, F., GOLDBLATT, D.
core  

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