scholarly journals Generalized pustular psoriasis with a novel mutation of interleukin-36 receptor antagonist, responding to methotrexate

2015 ◽  
Vol 1 (2) ◽  
pp. 51-53 ◽  
Author(s):  
Yee-Leng Teoh ◽  
Yong-Kwang Tay
2021 ◽  
pp. 247553032110517
Author(s):  
Avital Baniel ◽  
Efrat Bar-Ilan ◽  
Yuval Hilerowicz ◽  
Ilan Merdler ◽  
Eden Shkury ◽  
...  

Background Generalized pustular psoriasis of von Zumbusch is a rare variant of psoriasis often accompanied by systemic, sometimes life-threatening, symptoms. Generalized pustular psoriasis sometimes arises in pregnancy. Case report A 31-year-old female, with a history of schizophrenia and recurrent episodes of gestation-associated pustular psoriasis, was admitted to our department because of a generalized pustular rash during the 22nd week of her fifth pregnancy. Clinical and histopathological examinations were suggestive of generalized pustular psoriasis (von Zumbusch type). During this hospitalization, she developed acute dyspnea, fever, tachycardia, and marked leukocytosis. An extensive workup failed to reveal an infectious, cardiac, or pulmonary abnormality, while severe respiratory distress necessitated mechanical ventilation. Radio-imaging revealed diffuse alveolar infiltrates consistent with acute respiratory distress syndrome (ARDS). In the absence of any other plausible cause, ARDS was considered as secondary to her skin disease. Genetic base was suspected, and genetic analysis uncovered a novel mutation in IL36RN encoding the IL-36 receptor antagonist. Only 15 cases of ARDS secondary to psoriasis have been described to date. This is the first report of this very rare complication in a known carrier of an IL36RN mutation. The fact that IL36RN is abundantly expressed in the lung as well as in the epidermis may underlie the unusual clinical features of this dramatic case. Conclusion The present case suggests the need to carefully monitor patients with pregnancy-associated generalized pustular psoriasis for possible life-threatening pulmonary complications and the possible link to IL36RN mutation.


2015 ◽  
Vol 7 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Chiharu Tominaga ◽  
Masaaki Yamamoto ◽  
Yasutomo Imai ◽  
Kiyofumi Yamanishi

A 78-year-old woman who had been suffering from psoriasis vulgaris for 31 years was admitted to hospital because of her erythroderma. A toxic eruption was suspected and she was treated with prednisolone 30 mg daily. However, it was ineffective and, suspecting psoriatic erythroderma, cyclosporine 150 mg daily was administered with tapering of the prednisolone. Two weeks after a dose reduction of cyclosporine to 100 mg/day, erythroderma with widespread generalized pustules and fever developed. Histology of a biopsy revealed inflammatory infiltrates in the skin with a spongiform pustule of Kogoj, which was consistent with generalized pustular psoriasis (GPP). Her pustules improved with additional etretinate 20 mg/day, but the erythroderma persisted and she consulted us. Three sessions of granulocyte and monocyte apheresis once weekly were effective for her condition and decreased her serum levels of IL-6 and IL-8. She had homozygous mutations of c.[28C>T] in IL36RN which cause p.[Arg10Ter]. She is the oldest reported case of GPP with a deficiency of interleukin-36 receptor antagonist (DITRA), although GPP in DITRA has been suggested to usually occur in younger cases with no pre-existing psoriasis vulgaris.


2011 ◽  
Vol 365 (7) ◽  
pp. 620-628 ◽  
Author(s):  
Slaheddine Marrakchi ◽  
Philippe Guigue ◽  
Blair R. Renshaw ◽  
Anne Puel ◽  
Xue-Yuan Pei ◽  
...  

2013 ◽  
Vol 133 (11) ◽  
pp. 2514-2521 ◽  
Author(s):  
Kazumitsu Sugiura ◽  
Akemi Takemoto ◽  
Michiya Yamaguchi ◽  
Hidetoshi Takahashi ◽  
Yukiko Shoda ◽  
...  

Medicine ◽  
2020 ◽  
Vol 99 (45) ◽  
pp. e23068
Author(s):  
Zhi-Jie Liu ◽  
Yu-Tong Tian ◽  
Bo-Yi Shi ◽  
Yin Zhou ◽  
Xue-Song Jia

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