E-ISSN 2534-9821
 

Case Report
Online Published: 14 May 2021
 


Von Recklinghausen’s Disease: Case Report and Review of Literature

Siswanto Wahab, Welly Wijayanti, Sri Rimayani, Faridha Ilyas, Nurelly Waspodo, Farida Tabri.


Abstract
Neurofibromatosis type 1 (NF-1), formerly known as von Recklinghausen disease, is an autosomal dominant multisystem disorder characterized by skin manifestations, skeletal abnormalities and nervous system involvement. A typical case with a prevalence of 1: 2500 to 1: 3500 people, this case report can also be expected to provide additional insight. We report a case of a 14-year-old girl with complaints of skin and soft lumps in almost all body parts for the past 8 years. The appearance of multiple lenticular to plaque size café-au-lait macules since the age of one. In the gluteus region, plexiform neurofibroma is found with indistinct borders. The histopathological result supports the diagnosis of neurofibromatosis. The patient was also consulted by an ophthalmologist and found Lisch’s nodules in the left eye. Lumbosacral AP/ lateral radiography showed dextro-convex lumbar scoliosis. Based on the National Institutes of Health conference in 1987, NF-1 can be diagnosed when two or more out of seven diagnostic criteria are met. The patient was diagnosed with NF-1 and received surgical excision therapy.

Key words: Neurofibroma, Neurofibromatosis type 1, von Recklinghausen


 
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How to Cite this Article
Pubmed Style

Wahab S, Wijayanti W, Rimayani S, Ilyas F, Waspodo N, Tabri F. Von Recklinghausen’s Disease: Case Report and Review of Literature. Int J Med Rev Case Rep. 2021; 5(2): 80-84. doi:10.5455/IJMRCR.Von-Recklinghausen-Disease-172-1606638753


Web Style

Wahab S, Wijayanti W, Rimayani S, Ilyas F, Waspodo N, Tabri F. Von Recklinghausen’s Disease: Case Report and Review of Literature. https://www.mdpub.net/?mno=15133 [Access: October 13, 2024]. doi:10.5455/IJMRCR.Von-Recklinghausen-Disease-172-1606638753


AMA (American Medical Association) Style

Wahab S, Wijayanti W, Rimayani S, Ilyas F, Waspodo N, Tabri F. Von Recklinghausen’s Disease: Case Report and Review of Literature. Int J Med Rev Case Rep. 2021; 5(2): 80-84. doi:10.5455/IJMRCR.Von-Recklinghausen-Disease-172-1606638753



Vancouver/ICMJE Style

Wahab S, Wijayanti W, Rimayani S, Ilyas F, Waspodo N, Tabri F. Von Recklinghausen’s Disease: Case Report and Review of Literature. Int J Med Rev Case Rep. (2021), [cited October 13, 2024]; 5(2): 80-84. doi:10.5455/IJMRCR.Von-Recklinghausen-Disease-172-1606638753



Harvard Style

Wahab, S., Wijayanti, . W., Rimayani, . S., Ilyas, . F., Waspodo, . N. & Tabri, . F. (2021) Von Recklinghausen’s Disease: Case Report and Review of Literature. Int J Med Rev Case Rep, 5 (2), 80-84. doi:10.5455/IJMRCR.Von-Recklinghausen-Disease-172-1606638753



Turabian Style

Wahab, Siswanto, Welly Wijayanti, Sri Rimayani, Faridha Ilyas, Nurelly Waspodo, and Farida Tabri. 2021. Von Recklinghausen’s Disease: Case Report and Review of Literature. International Journal of Medical Reviews and Case Reports, 5 (2), 80-84. doi:10.5455/IJMRCR.Von-Recklinghausen-Disease-172-1606638753



Chicago Style

Wahab, Siswanto, Welly Wijayanti, Sri Rimayani, Faridha Ilyas, Nurelly Waspodo, and Farida Tabri. "Von Recklinghausen’s Disease: Case Report and Review of Literature." International Journal of Medical Reviews and Case Reports 5 (2021), 80-84. doi:10.5455/IJMRCR.Von-Recklinghausen-Disease-172-1606638753



MLA (The Modern Language Association) Style

Wahab, Siswanto, Welly Wijayanti, Sri Rimayani, Faridha Ilyas, Nurelly Waspodo, and Farida Tabri. "Von Recklinghausen’s Disease: Case Report and Review of Literature." International Journal of Medical Reviews and Case Reports 5.2 (2021), 80-84. Print. doi:10.5455/IJMRCR.Von-Recklinghausen-Disease-172-1606638753



APA (American Psychological Association) Style

Wahab, S., Wijayanti, . W., Rimayani, . S., Ilyas, . F., Waspodo, . N. & Tabri, . F. (2021) Von Recklinghausen’s Disease: Case Report and Review of Literature. International Journal of Medical Reviews and Case Reports, 5 (2), 80-84. doi:10.5455/IJMRCR.Von-Recklinghausen-Disease-172-1606638753