Volume 50, Issue 7 pp. 906-911
ORIGINAL ARTICLE

Analysis of cytokine profiles in sera of single and multiple infantile hemangioma

Mariko Sakata

Mariko Sakata

Department of Dermatology, Wakayama Medical University, Wakayama, Japan

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Kayo Kunimoto

Corresponding Author

Kayo Kunimoto

Department of Dermatology, Wakayama Medical University, Wakayama, Japan

Correspondence

Kayo Kunimoto, Department of Dermatology, Wakayama Medical University, 811-1 Kimiidera, Wakayama, Wakayama 641-0012, Japan.

Email: [email protected]

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Ami Kawaguchi

Ami Kawaguchi

Department of Dermatology, Wakayama Medical University, Wakayama, Japan

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Yutaka Inaba

Yutaka Inaba

Department of Dermatology, Wakayama Medical University, Wakayama, Japan

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Chikako Kaminaka

Chikako Kaminaka

Department of Dermatology, Wakayama Medical University, Wakayama, Japan

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Yuki Yamamoto

Yuki Yamamoto

Department of Dermatology, Wakayama Medical University, Wakayama, Japan

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Nobuyuki Kakimoto

Nobuyuki Kakimoto

Department of Pediatrics, Wakayama Medical University, Wakayama, Japan

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Tomohiro Suenaga

Tomohiro Suenaga

Department of Pediatrics, Wakayama Medical University, Wakayama, Japan

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Daisuke Tokuhara

Daisuke Tokuhara

Department of Pediatrics, Wakayama Medical University, Wakayama, Japan

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Masatoshi Jinnin

Masatoshi Jinnin

Department of Dermatology, Wakayama Medical University, Wakayama, Japan

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First published: 27 March 2023
Citations: 1

Abstract

Infantile hemangiomas (IH) are benign vascular tumors that are common in infancy. They vary in growth, size, location, and depth, and although most lesions are relatively small, approximately one fifth of patients have multiple lesions. Risk factors for IH include female sex, low birth weight, multiple gestation, preterm birth, progesterone therapy, and family history, but the mechanism that causes multiple lesions is unclear. We hypothesized that blood cytokines are involved as a cause of multiple IHs, and tried to prove this using sera and membrane arrays from patients with single and multiple IHs. Serum samples were obtained from five patients with multiple lesions and four patients with a single lesion, none of which had received any treatment. Serum levels of 20 cytokines were measured using human angiogenesis antibody membrane array. Four of the 20 cytokines (bFGF, IFN-γ, IGF-I, and TGF-β1) were higher in the patients with multiple lesions than in those with single lesion, with statistically significant difference (p < 0.05). Notably, signal for IFN-γ was evident in all cases with multiple IHs, but was absent in cases with single IH. Although not significant, there was mild correlation between IFN-γ and IGF-I (r = 0.64, p = 0.065), and between IGF-I and TGF-β1 (r = 0.63, p = 0.066). bFGF levels were strongly and significantly correlated with the number of lesions (r = 0.88, p = 0.0020). In conclusion, blood cytokines could act as a cause of multiple IHs. This is a pilot study with a small cohort, so further large-scale studies are necessary.

CONFLICT OF INTEREST STATEMENT

The authors report no conflicts of interest in relation to this article.

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