Cholinesterases in Neurofibromas

Winkelmann, R. K.

doi:10.1001/archderm.1962.01590010112014

Search citation statements

Order By: Relevance

Paper Sections

Select...

Discussion1

Besprechung1

Citation Types

Supporting

Mentioning

Contrasting

Unclassified

Year Published

1962

2000

Publication Types

Select...

Article7

Relationship

Self Cite1

Independent6

Authors

Journals

Cited by 37 publications

(2 citation statements)

References 7 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…These tumors originate largely in the sheaths of somatic and vegetative nerves and their supporting structures. It was found recently that some of these growths contain a nonspecific cholinesterase-factor which is found only in tumors of neural origin (35). Not rarely other congenital malformations appear in patients with NF and in their families.…”

Section: Discussionmentioning

confidence: 99%

Myotonic Dystrophy, Acute Intermittent Porphyria and Neurofibromatosis in one Patient

Pruzanski¹,

Adler²

1966

Hum Hered

View full text Add to dashboard Cite

Section: Discussionmentioning

confidence: 99%

Myotonic Dystrophy, Acute Intermittent Porphyria and Neurofibromatosis in one Patient

Pruzanski¹,

Adler²

1966

Hum Hered

View full text Add to dashboard Cite

“…Nach dieser Hypothese ist eine Vererbung der SNF nicht zu befürchten, da die NF-Mutation nur in dem befallenen Segment vorliegt [20,25]. In 12 Fällen, inklusive der vorliegenden Kasuistik, wurden ausschließlich kutane bilaterale Neurofibrome beschrieben, wobei vorwiegend thorakolumbale Dermatome involviert waren [1,4,5,12,15,19,22,24,26,28]. Eine gonadale Mutation mit der Folge eines Keimbahnmosaiks kann die Vererbung einer SNF-Mutation erklären, wobei sich bei den Nachkommen eine diffuse systemische NF (NF-I) manifestiert.…”

Section: Besprechungunclassified

Bilaterale segmentale Neurofibromatose unter dem Bild eines epidermalen Nävus

Gambichler¹,

Kuster²,

Wolter

et al. 2000

Der Hautarzt

View full text Add to dashboard Cite

Neurofibromatosis is a neuroectodermal systemic disease. A rare variant of this condition is bilateral segmental neurofibromatosis. A 29-year-old man presented with bilateral papillomatous plaques in the lumbar dermatomes. Clinically, the lesions were very similar to an epidermal nevus but histologic examination revealed superficial neurofibromas. Family history, ophthalmologic and neurologic investigations were unremarkable. The unusual morphologic presentation of bilateral segmental neurofibromas in this case points to the wide clinical spectrum of the disease and the significance of histologic examination in systematic nevoid lesions.

show abstract