Volume 52, Issue 5-6 pp. 416-422

Microcystic variant of localized malignant mesothelioma accompanying an adenomatoid tumor-like lesion

Hajime Umezu

Hajime Umezu

Department of Surgical Pathology, Niigata University Hospital, Japan

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Kazuhisa Kuwata

Kazuhisa Kuwata

Second Department of Pathology, Niigata University School of Medicine, Niigata City, Japan

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Yusuke Ebe

Yusuke Ebe

Second Department of Pathology, Niigata University School of Medicine, Niigata City, Japan

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Takashi Yamamoto

Takashi Yamamoto

Second Department of Pathology, Niigata University School of Medicine, Niigata City, Japan

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Makoto Naito

Makoto Naito

Second Department of Pathology, Niigata University School of Medicine, Niigata City, Japan

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Yasushi Yamato

Yasushi Yamato

Second Department of Surgery, Niigata University School of Medicine, Niigata City, Japan and

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Takaaki Ishiyama

Takaaki Ishiyama

Second Department of Surgery, Niigata University School of Medicine, Niigata City, Japan and

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Masanori Tsuchida

Masanori Tsuchida

Second Department of Surgery, Niigata University School of Medicine, Niigata City, Japan and

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Mina Okuizumi

Mina Okuizumi

Department of Radiology, Niigata University School of Medicine, Niigata City, Japan

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Hiroshi Ishikawa

Hiroshi Ishikawa

Department of Radiology, Niigata University School of Medicine, Niigata City, Japan

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Naoya Koizumi

Naoya Koizumi

Department of Radiology, Niigata University School of Medicine, Niigata City, Japan

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First published: 11 July 2002
Citations: 36
Hajime Umezu, MD, Department of Surgical Pathology, Niigata University Hospital, Asahimachi-dori 1-754, Niigata City, 951-8510, Japan. Email: [email protected]

Abstract

The case of a 70-year-old man with a hitherto undescribed pleural mesothelioma is reported. The tumor was localized in the left lung apex and had invaded the parietal pleura. Histologically, the tumor was characterized by a proliferation of epithelioid cells and the formation of microcysts. The tumor cells were positive for calretinin and vimentin, and possessed abundant microvilli, indicating a mesothelial cell origin for the tumor. A high Ki-67 index and mitotic index, and the recurrence of the tumor after surgery, indicated malignancy. Based on the evidence, we propose that the tumor is a microcystic variant of a localized malignant mesothelioma.

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