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eISSN: 2084-9893
ISSN: 0033-2526
Dermatology Review/Przegląd Dermatologiczny
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SCImago Journal & Country Rank
2/2023
vol. 110
 
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abstract:
Case report

Lipoid proteinosis coexisting with rare psychiatric manifestations: a case report with a review of literature

Kritika Gupta
1
,
Hania Qamar Khan
1
,
Syed Suhail Amin
1
,
Iti Varshney
1
,
Saifullah Khalid
2
,
Murad Ahmed
3

  1. Department of Dermatology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, India
  2. Department of Radiodiagnosis, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, India
  3. Department of Pathology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, India
Dermatol Rev/Przegl Dermatol 2023, 110, 169–175
Online publish date: 2023/07/20
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Lipoid proteinosis is a rare autosomal recessive genodermatosis characterized by the deposition of hyaline material in the skin and internal organs. Skin involvement is in the form of blisters in infancy healing with pock-like scars, yellow waxy papules, plaques, moniliform blepharosis and diffuse infiltration. Neurological manifestations such as epilepsy, schizophrenia and memory loss have also been reported. We report the case of a 24-year-old female with lipoid proteinosis with neuro-psychiatric symptoms. Her non-contrast computed tomography of the head showed symmetrical calcification involving bilateral medial temporal lobes. We also review the literature on previous publications of lipoid proteinosis cases with neuropsychiatric involvement.
keywords:

lipoid proteinosis, Urbach-Wiethe disease, schizophrenia



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