第128回集談会＋総会，第383回日皮会青森地方会
会場：弘前大学医学部コミュニケーションセンター

2018年の業績を追加しました。

1. Komori T, Dainichi T, Masuno Y, Otsuka A, Nakano H, Sawamura D, Ishida-Yamamoto A, and Kabashima K. The p.Glu477Lys mutation in Keratin 5 is not necessarily mortal in generalized severe epidermolysis bullosa simplex under intensive dressing care.
J Dermatol., in press.

12.Matsui A, Akasaka E, Rokunohe D, Matsuzaki Y, Sawamura D, Nakano H.The first Japanese case of familial porphyria cutanea tarda diagnosed by a UROD mutation.
J Dermatol Sci. 2019 Jan;93(1):65-67.

2019_JDS(93)_Matsui

11.Morimoto N, Shimizu A, Hattori M, Kuriyama Y, Nakano H, Ohnishi K. Dystrophic epidermolysis bullosa pruriginosa presenting with flagellate scarring lesions. Clin Exp Derm 2019; 44: e5-6.

10.Matsuzaki Y, Takahashi M, Minakawa S, Jin K, Nakano H, Sawamura D.Cutaneous collagenous vasculopathy induced by the vascular endothelial growth factorreceptor inhibitor axitinib.Int J Dermatol. 2018 Dec;57(12):e167-e169.

9. Morimoto N, Shimizu A, Hattori M, Kuriyama Y, Nakano H, Ohnishi K. Dystrophic epidermolysis bullosa pruriginosa with a flagellate scarring lesion.
Clin Exp Dermatol 2018, in press.

8. Yaginuma A, Itoh M, Akasaka E, Nakano H, Sawamura D, Nakagawa H, Asahina A. Novel mutation c.263A>G in the ACVRL1 gene in a Japanese patient with hereditary hemorrhagic telangiectasia 2.
J Dermatol 2018, in press.

7. Li  M, Nakano H, Higashi N, Saeki H. Incontinentia pigmenti in a Japanese newborn female with a novel frameshift mutation in the IKBKG gene.
J Dermatol, 2018 in press.

6. Ohyama A, Nakano H, Imanishi Y, Seto T, Tsuruta, Kousinn D, Fukai K. A novel missense mutation of the STS gene in two siblings with X-linked ichthyosis, complicated by short stature, bone density reduction, epilepsy, and cryptorchidism.
Clin Exp Dermatol, 2018 in press.

5. Korekawa A, Kaneko T, Nakano H, Sawamura D. Pyogenic granuloma-like Kaposi’s sarcoma on the first toe.
J Dermatol, 2018 in press.

4. Komori T, Dainichi T, Otsuka A, Nakano H, Sawamura D, Ishida-Yamamoto A, and Kabashima K. Mild dystrophic epidermolysis bullosa associated with homozygous gene mutation c.6216+5G>T in type VII collagen ultrastrucrurally suggestive of the decreased number of anchoring fibrils.
J Dermatol, 2018 in press.

3. Hattori M, Ishikawa O, Oikawa D, Amano H, Yasuda M, Kaira K, Ishida-Yamamoto A, Nakano H, Sawamura D, Terawaki S, Wakamatsu K, Tokunaga F, Shimizu A. In-frame Val²¹⁶ -Ser²¹⁷ deletion of KIT in mild piebaldism causes aberrant secretion and SCF response.
J Dermatol Sci 2018, in press.

2. Hattori M, Shimizu A, Nakano H, Ishikawa O.
Mild phenotype of junctional epidermolysis bullosa with pyloric atresia due to a novel mutation of the ITGB4 gene.
J Dermatol, 2018 in press.

1. Komori T, Dainichi T, Masuno Y, Otsuka A, Nakano H, Sawamura D, Ishida-Yamamoto A, and Kabashima K.
The p.Glu477Lys mutation in Keratin 5 is not necessarily mortal in generalized severe epidermolysis bullosa simplex under intensive dressing care.
J Dermatol, 2018 in press.

2017年の業績を追加しました。

28.  Hattori M, Shimizu A, Nakano H, Ishikawa O.
A mild phenotype of junctional epidermolysis bullosa with pyloric atresia due to a novel mutation of the ITGB4 gene.
J Dermatol, 2017. in press

27. Fujimori N, Komatsu M, Tanaka N, Iwaya M, Nakano H, Sugiura A, Yamazaki T, Shibata S, Iwaya Y, Muraki T, Ichikawa Y, Kimura T, Joshita S, Umemura T, Matsumoto A, Tanaka E. Cimetidine/lactulose therapy ameliorates erythropoietic protoporphyria-related liver injury.
Clin J Gastroenterol. 2017 Oct;10(5):452-458.

26. Yoshioka A, Fujiwara S, Kawano H, Nakano H, Nakano S, Matsui T, Katayama Y, Nishigori C. Late-onset Erythropoietic Protoporphyria Associated with Myelodysplastic Syndrome Treated with Azacitidine.
Acta Derm Venereol. 2017 Oct 23. [Epub ahead of print]

第14回加齢皮膚医学研究会（2018.8.25-26）のホームページを開設しました。https://14kareihifu-hirosaki.jimdo.com/

2017年の業績を追加しました。

 

2017年の業績を追加しました。

Murakami Y, Wataya-Kaneda M, Iwatani Y, Kubota T, Nakano H, Katayama I. A novel mutation of OCRL1 in Lowe syndrome with multiple epidermal cysts.
J Dermatol 2017, in press.

 

2017年の業績を追加しました。

Fujii A, Matsuyama K, Mizutani Y, Kanoh H, Nakano H, Seishima M.
Multiple familial trichoepithelioma with a novel mutation of CYLD gene. J Dermatol 2017, in press.

 

2017年の業績を追加しました。

Hattori M, Shimizu A, Oikawa D, Kamei K, Kaira K, Yamamoto A, Nakano H, Sawamura D, Tokunaga F, Ishikawa O. ER stress in the pathogenesis of pretibial dystrophic epidermolysis bullosa.
Br J Dermatol. in press.

Suzuki H, Kikuchi K, Fukuhara N, Nakano H, Aiba S. Case of late-onset erythropoietic protoporphyria with myelodysplastic syndrome who has homozygous IVS3-48C polymorphism in the ferrochelatase gene.
J Dermatol. in press.

 

28.  Hattori M, Shimizu A, Nakano H, Ishikawa O.
A mild phenotype of junctional epidermolysis bullosa with pyloric atresia due to a novel mutation of the ITGB4 gene.
J Dermatol, 2017. in press

27. Fujimori N, Komatsu M, Tanaka N, Iwaya M, Nakano H, Sugiura A, Yamazaki T, Shibata S, Iwaya Y, Muraki T, Ichikawa Y, Kimura T, Joshita S, Umemura T, Matsumoto A, Tanaka E. Cimetidine/lactulose therapy ameliorates erythropoietic protoporphyria-related liver injury.
Clin J Gastroenterol. 2017 Oct;10(5):452-458.

26. Yoshioka A, Fujiwara S, Kawano H, Nakano H, Nakano S, Matsui T, Katayama Y, Nishigori C.
Late-onset Erythropoietic Protoporphyria Associated with Myelodysplastic Syndrome Treated with Azacitidine.
Acta Derm Venereol. 2017. in press.

25. Akasaka E, Nakano H, Fukui T, Korekawa A, Aizu T, Sawamura D.
The first case of multiple pilomatricomas caused by somatic mutations of CTNNB1 without any associated disorder.
J Dermatol Sci. 2017 Nov;88(2):259-260.

24. Kuriyama Y, Hattori M, Mitsui T, Nakano H, Oikawa D, Tokunaga F, Ishikawa O, Shimizu A.
Generalized verrucosis caused by various human papillomaviruses in a patient with GATA2 deficiency.
J Dermatol. 2017. in press.

23. Nishikawa Y, Matsuzaki Y, Kimura K, Rokunohe A, Nakano H, Sawamura D.
Modulation of Stimulator of Interferon Genes (STING) Expression by Interferon-γ in Human Keratinocytes.
Biochem. Genet. 2017. in press.

22. Korekawa A, Nakajima K, Nakano H, Sawamura D.
Successful epithelialization of perianal infantile hemangioma, presenting as intractable ulcers, with application of protective colostomy powder.
J Dermatol. 2017; 44(10): e264-e265.

21. Jin K, Matsuzaki Y, Akasaka E, Korekawa A, Nakano H, Sawamura D.
Successful treatment of low-dose methotrexate in combination with systemic steroids for juvenile multiple and symmetrical circumscribed morphea.
J Dermatol. 2017; 44(10): e256-e257.

20. Araki Y, Abe Y, Takeda Y, Nakano H, Sawamura D, Yamashita H, Suzuki T.
Incontinentia pigmenti with retinal vascular anomaly and deletion of exons 4-10 in NEMO.
J Dermatol. 2017; 44(8): 976-977.

19. Matsuzaki Y, Kaneko T, Makita E, Rokunohe A, Minakawa S, Nakano H, Sawamura D. Postoperative maxillary cyst presenting as a skin tumour on the cheek.
Eur J Dermatol. 2017; 27(4): 433-434.

18. Nakajima K, Jin K, Kaneko T, Matsuzaki Y, Aizu T, Nakano H, Sawamura D.
Cholesterotic fibrous histiocytoma with no associated dyslipidemia.
Int J Dermatol. 2017; 56(6): e124-e126.

17.Matsuzaki Y, Yokoyama S, Rokunohe A, Minakawa S, Nakano H, Sawamura D.
Successful treatment of Kyrle disease with narrowband ultraviolet B.
J Dermatol. 2017; 44(6): 721-722.

16. Korekawa A, Nakajima K, Makita E, Nakano H, Sawamura D.
External chalazion as reddish and intractable lower eyelid nodules in a child.
J Dermatol. 2017; 44(5): e93-e94.

15. Li M, Higashi N, Nakano H, Saeki H.
An ATP2A2 Missense Mutation in a Japanese Family with Darier Disease: A Case Report and Review of the Japanese Darier Disease Patients with ATP2A2 Mutations.
J Nippon Med Sch. 2017; 84(5): 246-250.

14. Mizawa M, Makino T, Furukawa F, Torai R, Nakano H, Sawamura D, Shimizu T.
The 6-year follow-up of a Japanese patient with silent erythropoietic protoporphyria.
JAAD Case Rep. 2017; 3(3): 169-171.

13. Murakami Y, Sakai S, Takeda K, Sawamura D, Yoshida K, Hirose T, Ikeda C, Mani H, Yamamoto T, Ito A.
Autistic traits modulate the activity of the ventromedial prefrontal cortex in response to female faces.
Neurosci Res. 2017: S0168-0102(17)30467-30464.

12. Toyonaga E, Nishie W, Izumi K, Natsuga K, Ujiie H, Iwata H, Yamagami J, Hirako Y, Sawamura D, Fujimoto W, Shimizu H. C-Terminal Processing of Collagen XVII Induces Neoepitopes for Linear IgA Dermatosis Autoantibodies.
J Invest Dermatol. 2017; 137(12): 2552-2559.

11. Matsuzaki Y, Rokunohe A, Minakawa S, Nomura K, Nakano H, Ito E, Sawamura D.
Incontinentia pigmenti in a male (XY) infant with long-term follow up over 8 years.
J Dermatol. 2017 in press.

10. Fukui T, Kitamura H, Harada K, Nakano H, Sawamura D.  Trichoscopic Findings of Erosive Pustular Dermatosis of the Scalp Associated with Gefitinib.
Case Rep Dermatol. 2017; 9(2): 44-49.

9. Minakawa S, Kaneko T, Matsuzaki Y, Yamada M, Kayaba H, Sawamura D.
Psoriasis Area and Severity Index is closely related to serum C-reactive protein level and neutrophil to lymphocyte ratio in Japanese patients.
J Dermatol. 2017; 44(10): e236-e237.

8. Takadama S, Nakaminami H, Aoki S, Akashi M, Wajima T, Ikeda M, Mochida A, Shimoe F, Kimura K, Matsuzaki Y, Sawamura D, Inaba Y, Oishi T, Nemoto O, Baba N, Noguchi N.
Prevalence of skin infections caused by Panton-Valentine leukocidin-positive methicillin-resistant Staphylococcus aureus in Japan, particularly in Ishigaki, Okinawa.
J Infect Chemother. 2017; 23(11): 800-803.

7. Akasaka E, Nakano H, Takagi Y, Toyomaki Y, Sawamura D. Multiple Milia as an Isolated Skin Manifestation of Dominant Dystrophic Epidermolysis Bullosa: Evidence of Phenotypic Variability.
Pediatr Dermatol. 2017; 34(2): e106-e108.

6. Matsui A, Kaneko T, Takiyoshi N, Rokunohe D, Nakano H, Sawamura D.
Juvenile temporal arteritis with eosinophilia associated with systemic sclerosis.
J Dermatol. 2017; 44(3): e50-e51.

5. Korekawa A, Nakajima K, Nakano H, Sawmura D.
Translucent basal cell carcinoma with a single cyst of the upper eyelid.
J Dermatol. 2017; 44(10): e264-e265.

4. Murakami Y, Wataya-Kaneda M, Iwatani Y, Kubota T, Nakano H, Katayama I.
Novel mutation of OCRL1 in Lowe syndrome with multiple epidermal cysts.
J Dermatol. 2017.  in press.

3. Fujii A, Matsuyama K, Mizutani Y, Kanoh H, Nakano H, Seishima M.M
ultiple familial trichoepithelioma with a novel mutation of CYLD gene.
J Dermatol 2017; 44(9): e228-e229.

2. Hattori M, Shimizu A, Oikawa D, Kamei K, Kaira K, Yamamoto A, Nakano H, Sawamura D, Tokunaga F, Ishikawa O.
ER stress in the pathogenesis of pretibial dystrophic epidermolysis bullosa.
Br J Dermatol. 2017; 177(4): e92-e93.

1.  Suzuki H, Kikuchi K, Fukuhara N, Nakano H, Aiba S.
Case of late-onset erythropoietic protoporphyria with myelodysplastic syndrome who has homozygous IVS3-48C polymorphism in the ferrochelatase gene.
J Dermatol. 2017; 44(6): 651-655.