𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Ectopic respiratory epithelium associated with multiple malformations

✍ Scribed by V. MAHLER; J. WURM; P.VON DEN DRIESCH

Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
590 KB
Volume
136
Category
Article
ISSN
0007-0963

No coin nor oath required. For personal study only.

✦ Synopsis

We report a patient with unique cutaneous plaques of ectopic respiratory epithelium. The epithelium was located superficially as raised erythematous plaques on the right lateral surface of the neck with some viscous secretion. Underlying branchial cysts or sinuses were excluded. The occurrence of ectopic respiratory epithelium was associated with congenital deafness and a hare-lip in our patient, suggesting multiple malformation during early embryonic development.

πŸ“œ SIMILAR VOLUMES

Ectopic bronchus: An insufficiently reco
Ectopic bronchus: An insufficiently recognized malformation causing respiratory morbidity in VATER association
✍ Hattori, Haruo; Okazaki, Shin; Higuchi, Yoshihisa; Yoshibayashi, Muneo; Yamamoto πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 12 KB

An 11-month-old boy presented with recurrent wheezing and atelectasis in the right upper lobe of the lung. Bronchoscopy and bronchography confirmed an ectopic bronchus arising from the right main bronchus. The diagnosis of VATER association was made on the basis of multiple vertebral and rib anomali

Chiari I malformation associated with ca
Chiari I malformation associated with callosal dysgenesis and ectopic neurohypophysis
✍ R.Nuri Sener πŸ“‚ Article πŸ“… 1995 πŸ› Elsevier Science 🌐 English βš– 242 KB

In patients with Chiari I malformation there usually is no anomaly of the supratentorial structures. In this communication we report a patient with Chiari I malformation, callosal dysgenesis, and an ectopic neurohypophysis. Both the splenium and the rostrum of the corpus callosum were hypoplastic, s

Ring chromosome 10 Associated with multi
Ring chromosome 10 Associated with multiple congenital malformations
✍ G. Simoni; F. Rossella; L. DalprΓ ; G. Visconti; C. Piria-Schwarz πŸ“‚ Article πŸ“… 1979 πŸ› Springer 🌐 English βš– 435 KB

A 46,XY,r(10) karyotype was found in lymphocytes and skin fibroblasts cultured from a 8-month-old male showing multiple malformations and severe mental retardation. A comparison of the clinical features observed in cases in which a 10 ring was identified by means of banding techniques has been also