𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Diencephalic syndrome and von recklinghausen's disease

✍ Scribed by Dr. Bruce Adornato; Bruce Berg

Publisher
John Wiley and Sons
Year
1977
Tongue
English
Weight
227 KB
Volume
2
Category
Article
ISSN
0364-5134

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

Two infants with von Recklinghausen's disease developed signs and symptoms of the diencephalic syndrome. Pathological examination confirmed the presence of hypothalamic tumors in both. The concurrence of these two entities, although previously unreported, is not unexpected given the incidence of intracranial tumor in von Recklinghausen's disease and the dinecephalic syndrome.

πŸ“œ SIMILAR VOLUMES

Testicular tumor concomitant with von Re
Testicular tumor concomitant with von Recklinghausen's disease
✍ Groot-Loonen, J. J. ;VoΓ»te, P. A. ;De Kraker, J. πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 166 KB

Neurofibromatosis or Von Recklinghau-nancies that did not originate from neurogenic tissue are also described. This paper provides the first documentation of a patient with neurofibromatosis and a mixed germ cell tumor of the testis. sen's disease is an autosomal dominant disorder, associated with

The relationship between nephroblastoma
The relationship between nephroblastoma and neurofibromatosis (Von Recklinghausen's disease)
✍ Ellsworth J. Stay; Gordon Vawter πŸ“‚ Article πŸ“… 1977 πŸ› John Wiley and Sons 🌐 English βš– 611 KB

Three cases with co-existent Wilm's tumor and Von Recklinghausen's Disease from a series of 342 nephroblastomas are discussed as to the significance of this association. Biological arguments favor a positive link because of the multiplicity of associative lesions which parallel each other, the co-ex

Disseminated neuroblastoma in a child wi
Disseminated neuroblastoma in a child with von recklinghausen's disease
✍ C. L. Witzleben; Richard A. Landy πŸ“‚ Article πŸ“… 1974 πŸ› John Wiley and Sons 🌐 English βš– 672 KB

Only two cases of coexisting von Recklinghausen's disease and neuroblastoma have been reported in the English literature, and in both the diagnosis of neurofibromatosis is somewhat tenuous. We report the case of a child with disseminated neuroblastoma who had a previous unequivocal diagnosis of von