| Literature DB >> 27450766 |
Naoko Takeo1, Sakuhei Fujiwara1, Takashi Sakai1, Tomoko Saito-Shono1, Kazushi Ishikawa1, Yutaka Hatano1.
Abstract
Hereditary lactate dehydrogenase (LDH) M-subunit deficiency is very rare and we have found reports of close to a dozen cases in the published work, two of which were associated with pustular psoriasis-like lesions. We report a third case of pustular psoriasis-like eruptions associated with LDH M-subunit deficiency, which occurred 24 years after the diagnosis of LDH M-subunit deficiency. These cases indicate that abnormal activity of LDH can induce pustular psoriatic lesions in the long term. Some patients with symptoms of hereditary LDH M-subunit deficiency have antecedent annular scaly plaque lesions, that resemble psoriatic lesions. We discuss a hypothesis to explain this scenario.Entities:
Keywords: zzm321990nicotinamide adenine dinucleotidezzm321990; lactate dehydrogenase; lactate dehydrogenase-M subunit deficiency; pellagra; pustular psoriasis
Mesh:
Substances:
Year: 2016 PMID: 27450766 DOI: 10.1111/1346-8138.13516
Source DB: PubMed Journal: J Dermatol ISSN: 0385-2407 Impact factor: 4.005