Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Solitary plexiform neurofibroma.

F G Aloi1, R Massobrio

  • 1Institute of Dermatology, University of Turin, Italy.

Dermatologica
|January 1, 1989
PubMed
Summary
This summary is machine-generated.

A solitary plexiform neurofibroma, a type of nerve sheath tumor, was diagnosed in a 35-year-old man. This case highlights that neurofibromatosis may present with a single lesion, even without other family history.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Ki67 antigen expression correlates with tumor progression and HLA-DR antigen expression in melanocytic lesions.

The Journal of investigative dermatology·1990
Same author

[Serum levels of soluble receptors of interleukin-2 in skin pathology].

Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia·1990
Same author

Cutaneous manifestations in T-zone lymphoma.

Current problems in dermatology·1990
Same author

Lymphoplasmocytoid lymphoma arising in herpes zoster scars.

Journal of the American Academy of Dermatology·1990
Same author

Hidrotic ectodermal dysplasia with diffuse eccrine syringofibroadenomatosis.

Archives of dermatology·1989
Same author

[Eccrine angiomatous nevus].

Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia·1989
Same journal

Radiodermatitis with late ulcer (sarcoma) for 34 years.

Dermatologica·2010
Same journal

Alopecia decalvans, totalis, maligna, with nail changes and tooth abnormalities.

Dermatologica·2010
Same journal

Epidermolysis bullosa tarda simplex.

Dermatologica·2010
Same journal

Blistering after psychological arousal.

Dermatologica·2010
Same journal

Mycosis fungoides in the tumor stage.

Dermatologica·2010
Same journal

Photoallergic rash after Irgafen.

Dermatologica·2010
See all related articles

Area of Science:

  • Dermatology
  • Oncology
  • Genetics

Background:

  • Neurofibromatosis, also known as von Recklinghausen's disease, is a genetic disorder characterized by the development of tumors along nerve pathways.
  • Plexiform neurofibromas are benign tumors that can grow within nerves and are often associated with neurofibromatosis.

Observation:

  • A case report of a 35-year-old male presenting with a solitary subcutaneous cord-like lesion on the abdominal wall.
  • Histological examination confirmed the lesion as a plexiform neurofibroma.

Findings:

  • Despite the plexiform neurofibroma being considered pathognomonic for neurofibromatosis, the patient and his family showed no other signs of the disease.
  • This suggests that neurofibromatosis can manifest as a solitary plexiform neurofibroma.

Related Experiment Videos

Implications:

  • This case broadens the understanding of the clinical presentation of neurofibromatosis.
  • It emphasizes the importance of considering solitary plexiform neurofibromas in the differential diagnosis of subcutaneous lesions, even in the absence of other stigmata of neurofibromatosis.
  • Further research may elucidate the genetic and clinical factors influencing solitary presentations of neurofibromatosis.