Results 61 to 70 of about 1,460 (178)

Coexisting orofacial granulomatosis with discoid lupus erythematosus: Report of a rare case

Indian Journal of Dermatopathology and Diagnostic Dermatology, 2018
Orofacial granulomatosis (OFG) comprises a group of diseases characterized by noncaseating granulomatous inflammation affecting the soft tissues of the oral and maxillofacial region.
Preema Sinha, Prince Yuvraj Singh, Arijit Sen, Aradhana Sood   +3 more
doaj   +1 more source

Morphea “en coup de sabre”: an unusual oral presentation [PDF]

, 2017
Morphea, or localized scleroderma, is an inflammatory disease that leads to sclerosis of the skin and underlying tissues due to excessive collagen deposition.
Esguep, Alfredo, Martínez, René, Marín, Constanza, Niklander, Sven   +3 more
core   +1 more source

From Kitchen to Inflammatory Bowel Disease (IBD) Clinic: Transforming the Role of Dietitians in IBD Care. A Narrative Review by Dietitians With Expertise in IBD

JCC Plus, Volume 1, Issue 1, January 2026.
Dietitians' role in inflammatory bowel disease (IBD) has expanded from supportive care to five pillars of specialised nutrition. Access and system barriers persist. The Dietitians of European Crohn's and Colitis Organisation propose a six‐step plan to formalise and expand the IBD dietitian role.
Alice S. Day, Julie Vanderstappen, Alicia Sandall, Vaios Svolos, Chen Sarbagili Shabat   +4 more
wiley   +1 more source

Invasive maxillary sinus aspergillosis: a case report successfully treated with voriconazole and surgical debridement [PDF]

, 2014
Introduction: Invasive aspergillosis of the paranasal sinuses is a rare disease and often misdiagnosed; however, its incidence has seen substancial growth over the past 2 decades. Definitive diagnosis of these lesions is based on histological examination
Peral Cagigal, B., Redondo González, L.M., Verrier Hernández, Alberto   +2 more
core   +1 more source

Plasma Cell Mucositis: A Differential Diagnosis–Oriented Case Report

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
We present the case of an 80‐year‐old woman who reported painful gingival swelling and bleeding gums persisting for 6 months. She had hypertension (treated with amlodipine and losartan), arrhythmia (digoxin), and hypothyroidism (levothyroxine). Examination revealed diffuse erythematous, fissured swelling with a cobblestone surface on the gingiva ...
Matías Klare Rojas, Victoria Rees Moral, René Jara Moya, Isidora Mujica Valenzuela, Sergio González Providell, Giuseppe Colella   +5 more
wiley   +1 more source

Granulomatous cheilitis: Report of three cases and systematic review of cases and case series reported from India

Clinical Dermatology Review, 2020
Introduction: Granulomatous cheilitis (GC) is a rare idiopathic inflammatory disorder characterized by chronic persistent swelling of the lips. Despite a lingering controversy, it remains linked to orofacial granulomatosis and Melkersson–Rosenthal ...
Yugal Kishore Sharma, Shivanti Chauhan, Kirti Deo, Prachi Agrawal   +3 more
doaj   +1 more source

Queilitis granulomatosa de Miescher [PDF]

, 2017
La queilitis granulomatosa es un raro proceso de etiología desconocida que se considera una forma oligosintomática del síndrome de Melkersson-Rosenthal.
Alsina Gibert, Mercè, Ferre Jorge, J., Malvehy, J. (Josep)   +2 more
core  

Re-diagnosed and Re-treated Orofacial Granulomatosis: A Case Report

Journal of Indian Academy of Oral Medicine and Radiology
Orofacial granulomatosis is an uncommon skin condition affecting the face and predominantly the lips, also referred to as cheilitis granulomatosa. We will be discussing a case of a 50-year-old female with a history of swollen lips for the past 3 years ...
Ahamed Ismail Samu Fathima, Sarumathi Thirugnanamurthy, Guruswathy Ravikumar, Kavitha Mathivanan   +3 more
doaj   +1 more source

Chronic granulomatous disease, the McLeod phenotype and the contiguous gene deletion syndrome-a review [PDF]

, 2011
Chronic Granulomatous Disease (CGD), a disorder of the NADPH oxidase system, results in phagocyte functional defects and subsequent infections with bacterial and fungal pathogens (such as Aspergillus species and Candida albicans). Deletions and missense,
Casey E Watkins, Eunkyung Song, Gayatri B Jaishankar, Guha Krishnaswamy, John Litchfield, Michelle Duffourc, Nikhil Holla, Niva Misra   +7 more
core   +3 more sources

Hereditary angioedema as a cause of recurrent abdominal pain in a pediatric patient with Crohn's disease

JPGN Reports, Volume 6, Issue 4, Page 465-468, November 2025.
Abstract Hereditary angioedema (HAE) is a rare genetic condition caused by deficient or dysfunctional C1 inhibitor protein (C1INH) resulting in episodic angioedema of the skin, upper airway, and gastrointestinal tract. HAE most often presents within the first two decades of life and may cause severe abdominal pain, nausea, diarrhea, and emesis, making ...
Stephanie L. Rager, Paula J. Busse, Joesph A. Picoraro   +2 more
wiley   +1 more source