Histopathological evaluation of the effectiveness of oral Eppikajutsuto treatment for lymphatic malformation

Space: StayCurrentMD Author: Shotaro Matsudera, Hanako Sato-Yazawa, Misao Terada, Takeshi Yamaguchi, Yukiko Tani, Shun Watanabe, Korehito Kashiwagi, Jun Ishii, Yoshifumi Ito, Kei Ogino, Kentaro Okamoto, Masanobu Nakajima, Shinji Morita, Satoru Yamaguchi, Hajime Kuroda, Takashi Tsuchi Published:

Author / Expert

Shotaro Matsudera, Hanako Sato-Yazawa, Misao Terada, Takeshi Yamaguchi, Yukiko Tani, Shun Watanabe, Korehito Kashiwagi, Jun Ishii, Yoshifumi Ito, Kei Ogino, Kentaro Okamoto, Masanobu Nakajima, Shinji Morita, Satoru Yamaguchi, Hajime Kuroda, Takashi Tsuchi

Topic overview

Abstract

Background

Lymphatic malformation (LM) is a congenital disease caused by lymphatic vessel malformation. Although standard therapies for LMs are sclerotherapy and/or surgical excision, a new therapy using Japanese herbal medicine Eppikajutsuto (TJ-28) has been recently reported as clinically effective. We aimed to experimentally confirm the therapeutic effectiveness of TJ-28 for LMs.

Methods

LM lesions were generated in the mesentery and peritoneum of mice by intraperitoneal injection of Freund's incomplete adjuvant. Mice with LMs were treated by gavage or dietary administration of TJ-28 for 2 months. Formalin-fixed paraffin-embedded tissue sections of mesentery and peritoneum tissues were histologically and immunohistochemically examined by focusing on lymph nodes and perinodal lymph vessels.

Results

Multiple Freund's incomplete adjuvant-associated foreign-body granulomas were formed in the mesentery and peritoneum, resulting in congestion of lymph fluid and dilatation of lymph vessels. The numbers and sizes of lymph nodes were not significantly different between TJ-28-treated and control groups. However, the luminal areas of lymphatic vessels were reduced significantly in the TJ-28 treatment group by both gavage and dietary administrations.

Conclusion

TJ-28 conspicuously reduced congestion of lymph fluid. This is the first histopathological evaluation of LM model mice to study the effectiveness of oral TJ-28 treatment.

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