Gingival Manifestations of Orofacial Granulomatosis: A Rare Finding

2017 ◽  
Vol 7 (2) ◽  
pp. 57-62
Author(s):  
Shalu Chandna ◽  
Aneet Mahendra ◽  
Ranveet Kaur
VASA ◽  
1999 ◽  
Vol 28 (4) ◽  
pp. 289-292 ◽  
Author(s):  
Tiesenhausen ◽  
Amann ◽  
Thalhammer ◽  
Aschauer

Congenital anomalies of the caval vein are often associated with other abnormities such as heart defects, situs inversus or a polysplenia-asplenia-syndrome. An isolated, congenital malformation like aplasia of the inferior vena cava is a rare finding. A review of the embryology and abnormities, diagnostics, clinical signs and treatment is given together with the histories of two patients having thrombosis of the lower extremities and pelvic veins, caused by aplasia of the inferior vena cava. After thrombotic complications caused by vena cava aplasia there is high risk of recurrence. Those patients should be anticoagulated for lifetime.


2016 ◽  
Vol 5 (1) ◽  
pp. 80-85 ◽  
Author(s):  
Esther A Hullah ◽  
Michael P Escudier

Orofacial granulomatosis (OFG) is a condition manifesting clinically with chronic swelling of the mouth and/or face, notably with swelling of the lips and oral mucosa, a full-thickness, erythematous gingivitis and mucosal ulceration of various clinical types.1 Some patients may also present with neurological findings, for example facial palsy. Biopsy of affected tissue shows lymphoedema, with or without granulomatous inflammation. The oral lesions in OFG are histologically indistinguishable from the oral lesions in Crohn's disease (CD) and other systemic granulomatous disorders. It is a condition which may respond to the exclusion of certain food-related chemicals from the diet in up to 60% of patients and, as such, is distinct from gastrointestinal CD.2 CD is a relapsing systemic inflammatory disease which predominantly affects the gut, and patients suffering from this disease frequently present with abdominal pain, fever and altered bowel habit.3 A proportion of patients with clinical OFG (without other systemic disease) may have asymptomatic gastrointestinal involvement or go on to develop gut CD2,4 suggesting an association between the two diseases. It is estimated that 1% of CD sufferers may have a diagnosis of OFG, but the majority of patients in specialist OFG clinics do not have gut symptoms.2


2005 ◽  
Vol 71 (6) ◽  
pp. 526-527 ◽  
Author(s):  
Gabriel Akopian ◽  
Magdi Alexander

Many surgeons are familiar with Amyand hernia, which is an inguinal hernia sac containing an appendix. However, few surgeons know of the contribution of Rene Jacques Croissant de Garengeot, an 18th century Parisian surgeon, to hernias. He is quoted in the literature as the first to describe the appendix in a femoral hernia sac. We discuss the case of an 81-year-old woman who presented with appendicitis within a femoral hernia, a rare finding at surgery that is almost never diagnosed preoperatively. We also propose crediting Croissant de Garengeot by naming this condition after him. Although his full last name is Croissant de Garengeot, for convenience we suggest the simple diagnosis of “de Garengeot hernia.”


Morphologie ◽  
2021 ◽  
Author(s):  
Thaís Amanda Frank de Almeida Alves ◽  
Marco Antonio Alves Braun ◽  
Márcio Luís Duarte ◽  
Lucas Ribeiro dos Santosc

2021 ◽  
Author(s):  
Andriy Hordiychuk ◽  
David S. C. Soon ◽  
Fiona M. Y. Lee

2020 ◽  
pp. 1-5
Author(s):  
Jalal Maghfour ◽  
Jennifer Kane ◽  
Leslie Robinson-Bostom ◽  
John Kawaoka ◽  
Nathaniel Jellinek
Keyword(s):  

2018 ◽  
pp. bcr-2018-226789
Author(s):  
Mantu Jain ◽  
Amit Tirpude
Keyword(s):  

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