A Case Report of Lipoid Proteinosis with Brain and Laryngeal Presentation

AuthorMohammad Ali Kazemien
AuthorZahra Ahmadian Mazhinen
AuthorHashem Sharifianen
AuthorSamira Hemmatien
AuthorBehnaz Moradien
OrcidBehnaz Moradi [0000-0003-2698-4872]en
Issued Date2020-07-31en
AbstractLipoid proteinosis (LP) is a rare autosomal recessive genodermatosis. Genetic mutation leads to deposition of abnormal amounts of hyaline like material in the skin and viscera, which is the cause of clinical manifestations. It mostly involves the skin, intracranium, and the larynx. In this case report, we present a case with a long history of hoarseness. Imaging findings include bilateral true vocal cord (TVC) mucosal irregularity with hyperdense depositions, bilateral medial temporal amygdala parallel bean shape calcification (pathognomonic sign), and bilateral striatal (caudate and putamen) hypoattenuation. The patient also had multiple warty papules on the hands. Biopsy of the right TVC showed submucosal deposition of periodic acid-Schiff (PAS)-positive amorphous hyaline material and confirmed the diagnosis of lipoid proteinosis. Typical imaging findings especially in the brain could be very helpful in interpretation of laryngeal imaging findings in cases of lipoid proteinosis who manifest with long term voice changes and hoarseness.en
DOIhttps://doi.org/10.5812/iranjradiol.100906en
KeywordLipoid Proteinosis, Genodermatosis, Hoarsenessen
KeywordLarynxen
KeywordMedial Temporal Lobeen
KeywordPapuleen
PublisherBrieflandsen
TitleA Case Report of Lipoid Proteinosis with Brain and Laryngeal Presentationen
TypeCase Reporten

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