scholarly journals Congenital agenesis of unilateral parotid gland with ipsilateral type I first branchial cleft anomaly: A rare presentation

2014 ◽  
Vol 15 (1) ◽  
pp. 53-56 ◽  
Author(s):  
Tripti Maithani ◽  
Apoorva Pandey ◽  
Seema Acharya
Keyword(s):  
Parotid Gland ◽  
Type I ◽  
Rare Presentation ◽  
Branchial Cleft ◽  
Congenital Agenesis

scholarly journals First Branchial Cleft Anomalies: Rare Work Type I and Type II Entities

2021 ◽  
pp. 014556132110157
Author(s):  
Konstantinos Tarazis ◽  
Konstantinos Garefis ◽  
Maria Garefi ◽  
Vasilios Nikolaidis ◽  
Angelos Chatziavramidis ◽  
...  
Keyword(s):  
Parotid Gland ◽  
Type I ◽  
Type Ii ◽  
Branchial Cleft Anomalies ◽  
Branchial Cleft ◽  
Branchial Anomalies ◽  
Work Type

First branchial cleft anomalies (FBCAs) are the most infrequent malformations that occur during the development of the branchial apparatus, appearing in less than 8% of all branchial anomalies. Traditionally, they are classified into Work type I and II, depending on their origin. We present a pair of rare FBCAs: a case of a preauricular Work type I cyst with twin fistulae coursing toward the parotid gland and a Work type II cyst of significant dimensions.

scholarly journals Rare Presentation of the Type I Choledochal Cyst in a Young Adult

HPB ◽  
2021 ◽  
Vol 23 ◽  
pp. S352
Author(s):  
N.Y. Muppalla ◽  
S. Sankar
Keyword(s):  
Young Adult ◽  
Choledochal Cyst ◽  
Type I ◽  
Rare Presentation

scholarly journals The Gastrointestinal Stromal Tumors of It: A Rare Presentation of Neurofibromatosis Type I

Cureus ◽  
2021 ◽  
Author(s):  
Amit R Hudgi ◽  
Mohammad Azam ◽  
Muaaz Masood ◽  
Hafiz Muhammad Sharjeel Arshad ◽  
John Erikson L Yap
Keyword(s):  
Gastrointestinal Stromal Tumors ◽  
Neurofibromatosis Type ◽  
Type I ◽  
Neurofibromatosis Type I ◽  
Rare Presentation ◽  
Stromal Tumors

Primary Salivary Rhabdomyosarcoma in Childhood: A Rare Presentation

2021 ◽  
Author(s):  
Imane Mbarki
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Sarcoma ◽  
Parotid Gland ◽  
Head And Neck ◽  
The Body ◽  
Rare Presentation

Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in childhood. It is originated from embryonic mesenchyma and can arise anywhere in the body. Head and neck location accounts for 35% of all RMC locations. The parotid gland is very rarely affected. Because of this infrequent occurrence and the multiplicity of therapeutic means of management, we report a case a 5-year-old child which was diagnosed as parotid RMS.

Adult-onset glutaric aciduria type I: rare presentation of a treatable disorder

Neurogenetics ◽  
2020 ◽  
Vol 21 (3) ◽  
pp. 179-186
Author(s):  
Pınar Gelener ◽  
Mariasavina Severino ◽  
Sevda Diker ◽  
Kerem Teralı ◽  
Gulten Tuncel ◽  
...  
Keyword(s):  
Glutaric Aciduria Type ◽  
Type I ◽  
Adult Onset ◽  
Rare Presentation ◽  
Glutaric Aciduria ◽  
Glutaric Aciduria Type I

scholarly journals Bullosis Diabeticorum: Rare Presentation in a Common Disease

2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
Vineet Gupta ◽  
Neha Gulati ◽  
Jaya Bahl ◽  
Jaswinder Bajwa ◽  
Naveen Dhawan
Keyword(s):  
Sudden Onset ◽  
Common Disease ◽  
Type I ◽  
Rare Presentation ◽  
Diabetic Vasculopathy ◽  
Diabetes Mellitus Type I ◽  
Uncontrolled Diabetes ◽  
History Of ◽  
Skin Biopsies ◽  
Bullosis Diabeticorum

A 27-year-old African American male presented with a sudden onset of blisters. He had a past medical history of uncontrolled diabetes mellitus type I, diabetic vasculopathy, and neuropathy. The physical examination revealed nonerythematous skin denudations on both elbows and lateral aspect of arm bilaterally. Investigations which included skin biopsies confirmed the diagnosis of bullosis diabeticorum. The bullae were treated with hydrotherapy and healed with no complications in 4 weeks. We present this case to illustrate the rare occurrence of diabetic bulla in a diabetic patient especially with poor glycemic control. The case is also a reminder of the importance of diabetes screening in nondiabetic patients who are diagnosed with diabetic bulla.

scholarly journals S2117 The GIST of It: A Rare Presentation of Neurofibromatosis Type I

2020 ◽  
Vol 115 (1) ◽  
pp. S1116-S1117
Author(s):  
Mohammad U. Azam ◽  
Amit Hudgi ◽  
Muaaz Masood ◽  
Hafiz Muhammad Sharjeel Arshad ◽  
Isaac E. Perry ◽  
...  
Keyword(s):  
Neurofibromatosis Type ◽  
Type I ◽  
Neurofibromatosis Type I ◽  
Rare Presentation
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