Comparative performance of insulinoma-associated protein 1 (INSM1) and routine immunohistochemical markers of neuroendocrine differentiation in the diagnosis of endocrinemucin-producingsweat gland carcinoma
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Parra, Ourania
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机构:Dartmouth Hitchcock Med Ctr, Dept Pathol & Lab Med, Lebanon, NH 03766 USA
Parra, Ourania
Linos, Konstantinos
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机构:Dartmouth Hitchcock Med Ctr, Dept Pathol & Lab Med, Lebanon, NH 03766 USA
Linos, Konstantinos
Yan, Shaofeng
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机构:Dartmouth Hitchcock Med Ctr, Dept Pathol & Lab Med, Lebanon, NH 03766 USA
Yan, Shaofeng
Lilo, Mohammed
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机构:Dartmouth Hitchcock Med Ctr, Dept Pathol & Lab Med, Lebanon, NH 03766 USA
Lilo, Mohammed
LeBlanc, Robert E.
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机构:Dartmouth Hitchcock Med Ctr, Dept Pathol & Lab Med, Lebanon, NH 03766 USA
LeBlanc, Robert E.
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[1] Dartmouth Hitchcock Med Ctr, Dept Pathol & Lab Med, Lebanon, NH 03766 USA
Endocrine mucin-producing sweat gland carcinoma (EMPSGC) is a rare cutaneous adnexal malignancy with predilection for the eyelids of older adults. It must be distinguished from metastatic adenocarcinomas of extracutaneous origin and from benign adnexal proliferations on partial samples when a solid growth component and mucin production are not evident. Thus, demonstration of neuroendocrine differentiation can help to ensure a correct diagnosis. Insulinoma-associated protein 1 (INSM1) is a novel neuroendocrine marker that has recently shown greater sensitivity than synaptophysin (SYN) and chromogranin (CHR) in the diagnosis of various neuroendocrine neoplasms. We compared the performance of these three markers across 10 examples of EMPSGC. All EMPSGCs expressed INSM1. Eight of ten were also immunoreactive for SYN; however, INSM1 staining was generally more intense and stained a greater proportion of the tumor cells. CHR staining was weak and focal in most cases. INSM1 staining was present in hidrocystoma-like components of cystic EMPSGC. These findings suggest that INSM1 may be more sensitive than SYN and CHR and thus valuable for establishing a diagnosis of EMPSGC.
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Saitama Med Univ Int Med Ctr, Hidaka, Japan
Univ Yamanashi, Chuo, Japan
Nagoya Univ, Grad Sch Med, Nagoya, Aichi, Japan
Natl Hosp Org NHO Nagoya Med Ctr, Nagoya, Aichi, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Kawasaki, T.
Tashima, T.
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Saitama Med Univ Int Med Ctr, Hidaka, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Tashima, T.
Ryozawa, S.
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Saitama Med Univ Int Med Ctr, Hidaka, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Ryozawa, S.
Nakamura, Y.
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Saitama Med Univ Int Med Ctr, Hidaka, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Nakamura, Y.
Fujimoto, A.
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Saitama Med Univ Int Med Ctr, Hidaka, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Fujimoto, A.
Usami, Y.
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Saitama Med Univ Int Med Ctr, Hidaka, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Usami, Y.
Inozume, T.
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Univ Yamanashi, Chuo, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Inozume, T.
Saitoh, M.
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Univ Yamanashi, Chuo, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Saitoh, M.
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Kondo, T.
Enomoto, A.
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Nagoya Univ, Grad Sch Med, Nagoya, Aichi, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Enomoto, A.
Nagai, H.
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Natl Hosp Org NHO Nagoya Med Ctr, Nagoya, Aichi, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Nagai, H.
Taniyama, K.
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NHO Kure Med Ctr, Hiroshima, Japan
Chugoku Canc Ctr, Hiroshima, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Taniyama, K.
Muramatsu, C.
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Shiga Univ, Hikone, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
Muramatsu, C.
Kaira, K.
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Saitama Med Univ Int Med Ctr, Hidaka, JapanSaitama Med Univ Int Med Ctr, Hidaka, Japan
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Saitama Med Univ, Dept Pathol, Int Med Ctr, 1397-1 Yamane, Hidaka, Saitama 3501298, JapanSaitama Med Univ, Dept Pathol, Int Med Ctr, 1397-1 Yamane, Hidaka, Saitama 3501298, Japan
Kawasaki, Tomonori
Kaira, Kyoichi
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Saitama Med Univ, Dept Resp Med, Int Med Ctr, Hidaka, JapanSaitama Med Univ, Dept Pathol, Int Med Ctr, 1397-1 Yamane, Hidaka, Saitama 3501298, Japan