scholarly journals A case report of complete appendiceal duplication on the normal site of a single caecum: A new variant?

2020 ◽  
Vol 74 ◽  
pp. 168-172
Author(s):  
Allan Ngulube ◽  
Crispin O.M. Ntoto ◽  
Derek Matsika ◽  
Wedu Ndebele ◽  
Ngqabutho Sanders Dube ◽  
...  
Keyword(s):  
2013 ◽  
Vol 168 (2) ◽  
pp. e84-e85 ◽  
Author(s):  
Kristen Dazy ◽  
Daniel Walters ◽  
Christine Holland ◽  
James Baldwin

PEDIATRICS ◽  
1986 ◽  
Vol 78 (1) ◽  
pp. 172-174
Author(s):  
MARGARET A. KENNA ◽  
SYLVAN E. STOOL ◽  
SUSAN B. MALLORY

Epidermolysis bullosa is a rare genetically determined, dermatologic disease in which minor trauma causes blister formation.1 A new variant of hereditary epidermolysis bullosa, generalized atrophic benign epidermolysis bullosa, junctional form, has been recently reported.2 Airway involvement has not been a notable feature of this disease. We report the first case of an infant having benign junctional epidermolysis bullosa with laryngeal involvement. CASE REPORT An 11-month-old white boy with known junctional epidermolysis bullosa and mild stridor since birth was referred by his dermatologist for increasing stridor of 24 hours duration. He was initially thought to have croup; however, conservative treatment with mist and racemic epinephrine did not improve his symptoms.


2020 ◽  
Vol 44 (2) ◽  
pp. 127-129
Author(s):  
Avia Fux-Noy

Migration describes the movement of an unerupted tooth within the bone when normal eruption is prevented and the tooth leaves its normal site of development. This report describes a case of distal migration and ectopic eruption of the mandibular first premolar in an 8.5-year-old boy. Following early extraction of the primary second molar, the first premolar migrated distally through the extraction site of the primary second molar and erupted into occlusion just mesial of the permanent first molar.


Author(s):  
Mariana Lavrador ◽  
Adriana Lages ◽  
Araújo Bárbara ◽  
Barros Luísa ◽  
Isabel Paiva
Keyword(s):  

2011 ◽  
Vol 17 (3) ◽  
Author(s):  
Hassan Seirafi ◽  
Somayeh Khezri ◽  
Saeid Morowati ◽  
Kambiz Kamyabhesari ◽  
Mehdi Mirzaeipour ◽  
...  
Keyword(s):  

1997 ◽  
Vol 19 (2) ◽  
pp. 187-191 ◽  
Author(s):  
Tobias Back ◽  
Gisela Stoltenburg-Didinger ◽  
Christoph Ploner ◽  
Helga Meisel ◽  
Rolf Zschenderlein

2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Khalifa E. Sharquie ◽  
Adil A. Noaimi ◽  
Ali S. Alaboudi

Background. Cutting nerve during operations like saphenous vein grafting and knee joint surgery are common surgical procedures.Objective. To report cases of dermatitis at the site of neuropathy following skin incision for saphenous vein grafting and knee joint surgery.Patients and Methods. This case report work was done in the Department of Dermatology, Baghdad Teaching Hospital, during 2009-2010, seven cases were recorded, six following saphenous vein grafting and one case after knee surgery. Five males and two females, their ages ranged from 50 to 66 (58 ± 5.033223) years. Detailed history and full clinical examination were done for each patient regarding all points related to their conditions.Results. All cases presented around 2-3 months following the operation with dermatitis at the site of operational incision. The dermatitis appeared on one side of the operational scar and at area of neuropathy, and the rash did not cross to contralateral side. The dermatitis was well-defined plaque or patch erythematous slight scaly and nonitchy and subsided within few weeks with or without topical therapy.Conclusions. Neuropathy dermatitis is apparently a new variant of dermatitis that follows nerve cut during surgery.


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