Faculty Profiles - TAKEICHI Takuya

Papers - TAKEICHI Takuya

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An infant with generalized pustular psoriasis and geographic tongue had a heterozygous IL36RN mutation and IgG2 deficiency.

Oi R, Takeichi T, Okuno Y, Kojima D, Sugawara K, Kono M, Muramatsu H, Akiyama M

Journal of dermatological science 2018.2

Autoinflammatory keratinization diseases: An emerging concept encompassing various inflammatory keratinization disorders of the skin.

Akiyama M, Takeichi T, McGrath JA, Sugiura K

Journal of dermatological science 2018.2

A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi-Goutières and Singleton-Merten syndromes in a single patient. Reviewed International journal

T Takeichi, C Katayama, T Tanaka, Y Okuno, N Murakami, M Kono, K Sugiura, Y Aoyama, M Akiyama

The British journal of dermatology Vol. 178 ( 2 ) page： E111 - E113 2018.2

Multiple keratotic papules and plaques on the trunk in Cowden's disease with MALT lymphoma. Reviewed International journal

Sayaka Mizuno, Takuya Takeichi, Junichi Sato, Masanao Nakamura, Hidemi Goto, Kazumitsu Sugiura, Masashi Akiyama

The Journal of dermatology Vol. 45 ( 2 ) page： 238 - 240 2018.2

Trichothiodystrophy, complementation group A complicated with squamous cell carcinoma Reviewed

T. Takeichi, S. Tomimura, Y. Okuno, M. Hamada, M. Kono, K. Sugiura, M. Akiyama

Journal of the European Academy of Dermatology and Venereology Vol. 32 ( 2 ) page： E75 - E77 2018.2

Mild case of Hailey-Hailey disease caused by a novel ATP2C1 mutation.

Hanamura T, Takeichi T, Okuno Y, Ichikawa D, Kono M, Akiyama M

The Journal of dermatology 2018.1

Hailey-Hailey disease due to ATP2C1 splice site mutation, successfully treated with minocycline hydrochloride Reviewed

M. Kono, M. Niizawa, T. Takeichi, Y. Muro, M. Akiyama

Journal of the European Academy of Dermatology and Venereology Vol. 32 ( 1 ) page： E19 - E20 2018.1

Autoinflammatory keratinization diseases. Reviewed

Akiyama M, Takeichi T, McGrath JA, Sugiura K.

J Allergy Clin Immunol. Vol. 140 ( 6 ) page： 1545-1547 2017.12

Granulocyte and monocyte apheresis can control juvenile generalized pustular psoriasis with mutation of IL36RN Reviewed

Y. Koike, M. Okubo, T. Kiyohara, R. Fukuchi, Y. Sato, S. Kuwatsuka, T. Takeichi, M. Akiyama, K. Sugiura, A. Utani

British Journal of Dermatology Vol. 177 ( 6 ) page： 1732 - 1736 2017.12

Language：English Publishing type：Research paper (scientific journal)

© 2017 British Association of Dermatologists Patients with deficiency of interleukin-36 receptor antagonist (DITRA), due to mutation of IL36RN, exhibit psoriatic phenotypes, typically generalized pustular psoriasis (GPP). We report a paediatric patient with DITRA, whose cutaneous lesions varied from psoriasis vulgaris in infancy to annular pustular psoriasis with acute exacerbation to GPP at 13 years of age. Conventional systemic treatments for GPP, which include oral retinoids, ciclosporin and methotrexate, are controversial in paediatric cases, because of their adverse effects and uncertain long-term consequences. Granulocyte monocyte apheresis, a process associated with few adverse events, promptly controlled the GPP of our paediatric patient, and has potential as a suitable alternative treatment for paediatric patients with DITRA.

DOI： 10.1111/bjd.15509

Web of Science

Scopus

PubMed

Biallelic mutations in KDSR disrupt ceramide synthesis and result in a spectrum of keratinization disorders associated with thrombocytopenia. Reviewed

Takeichi T, Torrelo A, Lee JYW, Ohno Y, Lozano ML, Kihara A, Liu L, Yasuda Y, Ishikawa J, Murase T, Rodrigo AB, Fernández-Crehuet P, Toi Y, Mellerio J, Rivera J, Vicente V, Kelsell DP, Nishimura Y, Okuno Y, Kojima D, Ogawa Y, Sugiura K, Simpson MA, McLean WHI, Akiyama M, McGrath JA.

J Invest Dermatol. Vol. 137 ( 11 ) page： 2344-2353 2017.11

Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation. Reviewed

Takeichi T, Kobayashi A, Ogawa E, Okuno Y, Kataoka S, Kono M, Sugiura K, Okuyama R, Akiyama M.

Br J Dermatol. Vol. 177 ( 4 ) page： e133-e135 2017.10

A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation. Reviewed International journal

Takuya Takeichi, Katsuhiko Tsukamoto, Yusuke Okuno, Daiei Kojima, Michihiro Kono, Yasushi Suga, Masashi Akiyama

Journal of dermatological science Vol. 88 ( 1 ) page： 144 - 146 2017.10

Phosphorylated signal transducer and activator of transcription 3 in the epidermis in adult-onset Still's disease. Reviewed International journal

Takuya Takeichi, Naoki Watanabe, Yoshinao Muro, Shiho Teshigawara, Motoki Sato, Nobutaro Ban, Masashi Akiyama

The Journal of dermatology Vol. 44 ( 10 ) page： 1172 - 1175 2017.10

Language：English Publishing type：Research paper (scientific journal)

Adult-onset Still's disease (AOSD) is characterized by multiple systemic inflammation of unknown etiology. Although the typical eruption of AOSD is salmon-pink rheumatoid rash on the trunk and extremities, persistent pruritic papules and plaques have also been reported. Correlations between serum cytokines, including interleukin-6 and -18, and disease activity in AOSD have been reported. Activated signal transducer and activator of transcription 3 (STAT3) is transported into the nucleus, where it functions as a transcription factor that regulates genes involved in cell survival and inflammation. To assess whether STAT3 was phosphorylated in skin samples from AOSD patients, we conducted immunohistochemical analysis of affected and unaffected lesions from four AOSD patients in comparison with 10 normal controls. Quantitative analysis was conducted by measuring the ratio of epidermal keratinocytes with phosphorylated STAT3 (p-STAT3)-positive nuclei to total epidermal keratinocytes. p-STAT3 was found to be more strongly expressed in the nuclei in the epidermis of AOSD than in normal controls. Quantification of the data revealed significant differences in staining for p-STAT3 between AOSD and normal skin. Our findings suggest that phosphorylation of STAT3 may be a potential therapeutic target for AOSD.

DOI： 10.1111/1346-8138.13888

Web of Science

Scopus

PubMed

Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation

Takeichi T., Kobayashi A., Ogawa E., Okuno Y., Kataoka S., Kono M., Sugiura K., Okuyama R., Akiyama M.

BRITISH JOURNAL OF DERMATOLOGY Vol. 177 ( 4 ) page： E133-E135 2017.10

Abscopal Effect of Local Irradiation Treatment for Diffuse Large B-cell Lymphoma. Reviewed International journal

Yuri Hidaka, Takuya Takeichi, Yuichi Ishikawa, Mariko Kawamura, Masashi Akiyama

Acta dermato-venereologica Vol. 97 ( 9 ) page： 1140 - 1141 2017.10

Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR9C7. Reviewed

Takeichi T, Nomura T, Takama H, Kono M, Sugiura K, Watanabe D, Shimizu H, Simpson MA, McGrath JA, Akiyama M.

Br J Dermatol. Vol. 177 ( 3 ) page： e62-e64 2017.9

A Child with Epidermolytic Ichthyosis from a Parent with Epidermolytic Nevus: Risk Evaluation of Transmission from Mosaic to Germline. Reviewed International journal

Michihiro Kono, Yasushi Suga, Tomohiro Akashi, Yasutomo Ito, Takuya Takeichi, Yoshinao Muro, Masashi Akiyama

The Journal of investigative dermatology Vol. 137 ( 9 ) page： 2024 - 2026 2017.9

Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR9C7

Takeichi T., Nomura T., Takama H., Kono M., Sugiura K., Watanabe D., Shimizu H., Simpson M. A., McGrath J. A., Akiyama M.

BRITISH JOURNAL OF DERMATOLOGY Vol. 177 ( 3 ) page： E62-E64 2017.9

A case of lamellar ichthyosis due to a novel TGM1 mutation associated with Parkinson's disease. Reviewed International journal

Runa Morita-Adachi, Takuya Takeichi, Yusuke Okuno, Shinsuke Kataoka, Shimpei Hoshino, Masashi Akiyama

European journal of dermatology : EJD Vol. 27 ( 4 ) page： 438 - 439 2017.7

Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan Reviewed

T. Takeichi, K. Tanahashi, T. Taki, M. Kono, K. Sugiura, M. Akiyama

BRITISH JOURNAL OF DERMATOLOGY Vol. 177 ( 1 ) page： 290 - 292 2017.7

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Papers - TAKEICHI Takuya