Dermatorynchus geneae: A seldom-described first branchial arch deformity
نویسندگان
چکیده
منابع مشابه
Dermatorynchus geneae: A seldom-described first branchial arch deformity
INTRODUCTION This case report addresses dermatorynchus geneae, a seldom-described deformity of the first branchial arch. Two previous case reports discuss this clinical entity, both of them published in the 1970s. Bittmann and Søgaard were the first to report the case of a 1-month-old girl who presented with an unusual 2-cm growth on the skin overlying the zygoma. Histologic analysis of the les...
متن کاملBilateral Second Arch Branchial Fistula-A Case Report
Introduction: Branchial arch anomalies represent defects in embryological developments whereby parts of the branchial arch persist in the head and neck regions as sinuses, fistulas, or cysts. These anomalies usually present as a unilateral lesion in the head and neck of young adults and children, which are excised upon the emergence of complications. Case Report: Herei...
متن کاملRecurrent Enterolithiasis Small Bowel Obstruction: A Case Seldom Described
BACKGROUND Enterolithiasis of the small bowel is a rare phenomenon in humans although it has been frequently described in equines. Primary enteroliths have been described including those occurring secondary to conditions like Crohn's disease, small bowel diverticula, tuberculous or postoperative strictures, and blind loops but those occurring in an otherwise normal gut are exceedingly rare. Of ...
متن کاملThe second branchial arch: rheumatological manifestations.
In the course of normal development in man, the middle and largest part of the second branchial arch, the keratohyal cartilage, develops into a fibrous cord, the so-called stylohyoid ligament. Ossification takes place solely at its two ends, that is, in the hyoid bone and in the styloid process of the skull. In the present paper the significance for the clinical rheumatologist of some developme...
متن کاملClinical Approach to a Suspected Case of First Branchial Arch Syndrome
First branchial arch syndrome is a congenital disorder characterized by a wide spectrum of anomalies in the first branchial arch, mainly affecting the lower jaw, ear, or mouth, during early embryonic development. We sought to confirm a suspected case of this syndrome by making differential diagnosis and taking an intensive clinical approach. A 12-year-6-month-old girl with a horizontally impact...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: JAAD Case Reports
سال: 2015
ISSN: 2352-5126
DOI: 10.1016/j.jdcr.2015.06.006