Naotomo Kambe

特定教授 / Program-Specific Professor

Kyoto University

Japan

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About

Naotomo Kambe is a Program-Specific Professor at Kyoto University in Japan. His research areas include autoimmune and autoinflammatory diseases, with a focus on patient-reported outcomes, as well as clinical studies related to conditions such as Schnitzler syndrome and alopecia areata. Professor Kambe has published numerous articles that contribute to understanding the efficacy and safety of treatments for various dermatological conditions.

Articles (20)

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2025

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2021

Collaborators (9)

Hiroyasu Abe

Senior Lecturer

Wakayama Medical University

JAPAN

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Yuya TABUCHI

Kyoto University Hospital

JAPAN

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Takuro Hakata

Kyoto University

JAPAN

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Saeko Nakajima

特定准教授 / Program-Specific Associate Professor

Kyoto University

JAPAN

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Takashi Nomura

特定准教授 / Program-Specific Associate Professor

Kyoto University

JAPAN

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Yuzaburo Inoue

Associate professor/Lecturer

Chiba University

JAPAN

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Takayoshi Komatsu-Fujii

Kyoto University Hospital

JAPAN

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Kenji Kabashima

JAPAN

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Masahiro Hirata

Kyoto University Hospital

JAPAN

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Naotomo Kambe

Research Interests

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Articles (20)

A case of non‐uremic calciphylaxis in a patient with secondary hyperparathyroidism and panhypopituitarism

Consideration of useful patient-reported outcome measures to identify the unmet medical needs of children and adults with autoimmune and autoinflammatory diseases

Psoriasiform Dermatitis Following Kawasaki Disease: A Case Report and Literature Review

A case of refractory alopecia areata successfully treated by combining delgocitinib ointment with excimer laser

Neutrophils predominate as IL1B-expressing cells in Schnitzler syndrome: Insights from the SCan study to evaluate the efficacy and safety of canakinumab in Japanese patients

Investigator-initiated, multi-center, single-arm, open-label study of the effectiveness of canakinumab in Japanese patients with Schnitzler syndrome

Neutrophilic epitheliotropism, proposed as an auto‐inflammatory condition of neutrophilic urticarial dermatosis including Schnitzler syndrome, is also observed in Japanese cases

Proteasome inhibitor‐associated histiocytoid Sweet's syndrome: Clinical and histological similarities to Nakajo‐Nishimura syndrome suggest a potential mechanism

A case of post herpes zoster granulomatous dermatitis successfully treated with UVA1 phototherapy

Presence of immunoglobulin E‐expressing antibody‐secreting cells in the dermis close to bullous pemphigoid lesions

A case of Kimura disease with atopic dermatitis successfully treated with baricitinib

Summary of the current status of clinically diagnosed cases of Schnitzler syndrome in Japan

Interleukin-13 inhibition by tralokinumab reduces inducible T-cell costimulator-positive innate lymphoid cells in skin lesions of atopic dermatitis

Panniculitis in dermatomyositis: Two cases with antitranscriptional intermediary factor‐1 antibody as myositis‐specific antibody and review of the literature

Acquired idiopathic generalized anhidrosis following pembrolizumab treatment

A New Era with the Development of Cytokine-Based Therapy for Pruritus

Refractory serum immunoglobulin M elevation during anti‐interleukin (IL)‐1‐ or IL‐6‐targeted treatment in four patients with Schnitzler syndrome

Skin‐associated lymphoid tissue could be a sign of systemic disease: reply from authors

Hereditary angioedema with a novel mutation, c.1481G>C, in the SERPING1 gene

Sustained Surface ICAM-1 Expression and Transient PDGF-B Production by Phorbol Myristate Acetate-Activated THP-1 Cells Harboring Blau Syndrome-Associated <i>NOD2</i> Mutations.

Collaborators (9)

Hiroyasu Abe

Yuya TABUCHI

Takuro Hakata

Saeko Nakajima

Takashi Nomura

Yuzaburo Inoue

Takayoshi Komatsu-Fujii

Kenji Kabashima

Masahiro Hirata

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