Histopathological features and prognostic significance of the micropapillary pattern in lung adenocarcinoma
The micropapillary pattern is characterized by small papillary tufts with no fibrovascular core lying in spaces and has been reported as an aggressive variant of carcinoma in several organs. We investigated the histopathobiological properties of the micropapillary pattern with immunohistochemistry,...
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Published in | Modern pathology Vol. 21; no. 8; pp. 992 - 1001 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Elsevier Inc
01.08.2008
Nature Publishing Group US Elsevier Limited |
Subjects | |
Online Access | Get full text |
ISSN | 0893-3952 1530-0285 1530-0285 |
DOI | 10.1038/modpathol.2008.79 |
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Abstract | The micropapillary pattern is characterized by small papillary tufts with no fibrovascular core lying in spaces and has been reported as an aggressive variant of carcinoma in several organs. We investigated the histopathobiological properties of the micropapillary pattern with immunohistochemistry, serial sections, and electron microscopy in lung adenocarcinoma. We further analyzed its clinicopathological character and prognosis. The subjects included 383 adenocarcinoma cases, of which 184 (48%) were micropapillary pattern-positive and 199 (52%) were micropapillary pattern-negative. On histology, micropapillary tufts seemed to float in the alveolar space or spaces encased by connective tissues, whereas serial sections revealed that most tufts had continuity with other tufts and even with the main tumor. Positive staining for the adhesion molecules E-cadherin and Β-catenin suggested the preservation of tight adhesion, and electron microscopy showed the existence of intercellular junctions. Negative staining for laminin and loss of basement membrane as determined by electron microscopy suggest a loss of cell–matrix contact. Positive staining for Ki-67 indicates that cells constituting micropapillary tufts retained their proliferation potency. There were no CD34-positive cells in micropapillary tufts, and the loss of the vascular core was confirmed. In micropapillary pattern-positive cases, lymphatic invasion was identified significantly more frequently than in micropapillary pattern-negative cases (P<0.001), even at stageIA (without lymph node metastasis, N=197) (P<0.001). The 5-year and 10-year overall survival rates of the micropapillary pattern-positive stageIA group were 77.6 and 67.6%, respectively, which were significantly less than those of the micropapillary pattern-negative stageIA group (98.1 and 98.1%) (P=0.001). In conclusion, cells constituting the micropapillary pattern are likely to have acquired anchorage-independent growth and a potential for high malignancy. |
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AbstractList | The micropapillary pattern is characterized by small papillary tufts with no fibrovascular core lying in spaces and has been reported as an aggressive variant of carcinoma in several organs. We investigated the histopathobiological properties of the micropapillary pattern with immunohistochemistry, serial sections, and electron microscopy in lung adenocarcinoma. We further analyzed its clinicopathological character and prognosis. The subjects included 383 adenocarcinoma cases, of which 184 (48%) were micropapillary pattern-positive and 199 (52%) were micropapillary pattern-negative. On histology, micropapillary tufts seemed to float in the alveolar space or spaces encased by connective tissues, whereas serial sections revealed that most tufts had continuity with other tufts and even with the main tumor. Positive staining for the adhesion molecules E-cadherin and beta-catenin suggested the preservation of tight adhesion, and electron microscopy showed the existence of intercellular junctions. Negative staining for laminin and loss of basement membrane as determined by electron microscopy suggest a loss of cell-matrix contact. Positive staining for Ki-67 indicates that cells constituting micropapillary tufts retained their proliferation potency. There were no CD34-positive cells in micropapillary tufts, and the loss of the vascular core was confirmed. In micropapillary pattern-positive cases, lymphatic invasion was identified significantly more frequently than in micropapillary pattern-negative cases (P<0.001), even at stageIA (without lymph node metastasis, N=197) (P<0.001). The 5-year and 10-year overall survival rates of the micropapillary pattern-positive stageIA group were 77.6 and 67.6%, respectively, which were significantly less than those of the micropapillary pattern-negative stageIA group (98.1 and 98.1%) (P=0.001). In conclusion, cells constituting the micropapillary pattern are likely to have acquired anchorage-independent growth and a potential for high malignancy. The micropapillary pattern is characterized by small papillary tufts with no fibrovascular core lying in spaces and has been reported as an aggressive variant of carcinoma in several organs. We investigated the histopathobiological properties of the micropapillary pattern with immunohistochemistry, serial sections, and electron microscopy in lung adenocarcinoma. We further analyzed its clinicopathological character and prognosis. The subjects included 383 adenocarcinoma cases, of which 184 (48%) were micropapillary pattern-positive and 199 (52%) were micropapillary pattern-negative. On histology, micropapillary tufts seemed to float in the alveolar space or spaces encased by connective tissues, whereas serial sections revealed that most tufts had continuity with other tufts and even with the main tumor. Positive staining for the adhesion molecules E-cadherin and β -catenin suggested the preservation of tight adhesion, and electron microscopy showed the existence of intercellular junctions. Negative staining for laminin and loss of basement membrane as determined by electron microscopy suggest a loss of cell–matrix contact. Positive staining for Ki-67 indicates that cells constituting micropapillary tufts retained their proliferation potency. There were no CD34-positive cells in micropapillary tufts, and the loss of the vascular core was confirmed. In micropapillary pattern-positive cases, lymphatic invasion was identified significantly more frequently than in micropapillary pattern-negative cases ( P <0.001), even at stageIA (without lymph node metastasis, N =197) ( P <0.001). The 5-year and 10-year overall survival rates of the micropapillary pattern-positive stageIA group were 77.6 and 67.6%, respectively, which were significantly less than those of the micropapillary pattern-negative stageIA group (98.1 and 98.1%) ( P =0.001). In conclusion, cells constituting the micropapillary pattern are likely to have acquired anchorage-independent growth and a potential for high malignancy. The micropapillary pattern is characterized by small papillary tufts with no fibrovascular core lying in spaces and has been reported as an aggressive variant of carcinoma in several organs. We investigated the histopathobiological properties of the micropapillary pattern with immunohistochemistry, serial sections, and electron microscopy in lung adenocarcinoma. We further analyzed its clinicopathological character and prognosis. The subjects included 383 adenocarcinoma cases, of which 184 (48%) were micropapillary pattern-positive and 199 (52%) were micropapillary pattern-negative. On histology, micropapillary tufts seemed to float in the alveolar space or spaces encased by connective tissues, whereas serial sections revealed that most tufts had continuity with other tufts and even with the main tumor. Positive staining for the adhesion molecules E-cadherin and beta-catenin suggested the preservation of tight adhesion, and electron microscopy showed the existence of intercellular junctions. Negative staining for laminin and loss of basement membrane as determined by electron microscopy suggest a loss of cell-matrix contact. Positive staining for Ki-67 indicates that cells constituting micropapillary tufts retained their proliferation potency. There were no CD34-positive cells in micropapillary tufts, and the loss of the vascular core was confirmed. In micropapillary pattern-positive cases, lymphatic invasion was identified significantly more frequently than in micropapillary pattern-negative cases (P<0.001), even at stageIA (without lymph node metastasis, N=197) (P<0.001). The 5-year and 10-year overall survival rates of the micropapillary pattern-positive stageIA group were 77.6 and 67.6%, respectively, which were significantly less than those of the micropapillary pattern-negative stageIA group (98.1 and 98.1%) (P=0.001). In conclusion, cells constituting the micropapillary pattern are likely to have acquired anchorage-independent growth and a potential for high malignancy.The micropapillary pattern is characterized by small papillary tufts with no fibrovascular core lying in spaces and has been reported as an aggressive variant of carcinoma in several organs. We investigated the histopathobiological properties of the micropapillary pattern with immunohistochemistry, serial sections, and electron microscopy in lung adenocarcinoma. We further analyzed its clinicopathological character and prognosis. The subjects included 383 adenocarcinoma cases, of which 184 (48%) were micropapillary pattern-positive and 199 (52%) were micropapillary pattern-negative. On histology, micropapillary tufts seemed to float in the alveolar space or spaces encased by connective tissues, whereas serial sections revealed that most tufts had continuity with other tufts and even with the main tumor. Positive staining for the adhesion molecules E-cadherin and beta-catenin suggested the preservation of tight adhesion, and electron microscopy showed the existence of intercellular junctions. Negative staining for laminin and loss of basement membrane as determined by electron microscopy suggest a loss of cell-matrix contact. Positive staining for Ki-67 indicates that cells constituting micropapillary tufts retained their proliferation potency. There were no CD34-positive cells in micropapillary tufts, and the loss of the vascular core was confirmed. In micropapillary pattern-positive cases, lymphatic invasion was identified significantly more frequently than in micropapillary pattern-negative cases (P<0.001), even at stageIA (without lymph node metastasis, N=197) (P<0.001). The 5-year and 10-year overall survival rates of the micropapillary pattern-positive stageIA group were 77.6 and 67.6%, respectively, which were significantly less than those of the micropapillary pattern-negative stageIA group (98.1 and 98.1%) (P=0.001). In conclusion, cells constituting the micropapillary pattern are likely to have acquired anchorage-independent growth and a potential for high malignancy. The micropapillary pattern is characterized by small papillary tufts with no fibrovascular core lying in spaces and has been reported as an aggressive variant of carcinoma in several organs. We investigated the histopathobiological properties of the micropapillary pattern with immunohistochemistry, serial sections, and electron microscopy in lung adenocarcinoma. We further analyzed its clinicopathological character and prognosis. The subjects included 383 adenocarcinoma cases, of which 184 (48%) were micropapillary pattern-positive and 199 (52%) were micropapillary pattern-negative. On histology, micropapillary tufts seemed to float in the alveolar space or spaces encased by connective tissues, whereas serial sections revealed that most tufts had continuity with other tufts and even with the main tumor. Positive staining for the adhesion molecules E-cadherin and Β-catenin suggested the preservation of tight adhesion, and electron microscopy showed the existence of intercellular junctions. Negative staining for laminin and loss of basement membrane as determined by electron microscopy suggest a loss of cell–matrix contact. Positive staining for Ki-67 indicates that cells constituting micropapillary tufts retained their proliferation potency. There were no CD34-positive cells in micropapillary tufts, and the loss of the vascular core was confirmed. In micropapillary pattern-positive cases, lymphatic invasion was identified significantly more frequently than in micropapillary pattern-negative cases (P<0.001), even at stageIA (without lymph node metastasis, N=197) (P<0.001). The 5-year and 10-year overall survival rates of the micropapillary pattern-positive stageIA group were 77.6 and 67.6%, respectively, which were significantly less than those of the micropapillary pattern-negative stageIA group (98.1 and 98.1%) (P=0.001). In conclusion, cells constituting the micropapillary pattern are likely to have acquired anchorage-independent growth and a potential for high malignancy. |
Author | Kawamura, Masafumi Douguchi, Junya Horinouchi, Hirohisa Hashiguchi, Akinori Hayashi, Yuichiro Watanabe, Masazumi Shimada, Naoki Sakamoto, Michiie Kamiya, Kazunori Yamada, Taketo Izumi, Yotaro Kobayashi, Koichi |
Author_xml | – sequence: 1 givenname: Kazunori surname: Kamiya fullname: Kamiya, Kazunori organization: Department of Pathology, School of Medicine, Keio University, Tokyo, Japan – sequence: 2 givenname: Yuichiro surname: Hayashi fullname: Hayashi, Yuichiro organization: Department of Pathology, School of Medicine, Keio University, Tokyo, Japan – sequence: 3 givenname: Junya surname: Douguchi fullname: Douguchi, Junya organization: Department of Pathology, School of Medicine, Keio University, Tokyo, Japan – sequence: 4 givenname: Akinori surname: Hashiguchi fullname: Hashiguchi, Akinori organization: Department of Pathology, School of Medicine, Keio University, Tokyo, Japan – sequence: 5 givenname: Taketo surname: Yamada fullname: Yamada, Taketo organization: Department of Pathology, School of Medicine, Keio University, Tokyo, Japan – sequence: 6 givenname: Yotaro surname: Izumi fullname: Izumi, Yotaro organization: Department of Surgery, Division of General Thoracic Surgery, School of Medicine, Keio University, Tokyo, Japan – sequence: 7 givenname: Masazumi surname: Watanabe fullname: Watanabe, Masazumi organization: Department of Surgery, Division of General Thoracic Surgery, School of Medicine, Keio University, Tokyo, Japan – sequence: 8 givenname: Masafumi surname: Kawamura fullname: Kawamura, Masafumi organization: Department of Surgery, Division of General Thoracic Surgery, School of Medicine, Keio University, Tokyo, Japan – sequence: 9 givenname: Hirohisa surname: Horinouchi fullname: Horinouchi, Hirohisa organization: Department of Surgery, Division of General Thoracic Surgery, School of Medicine, Keio University, Tokyo, Japan – sequence: 10 givenname: Naoki surname: Shimada fullname: Shimada, Naoki organization: Department of Preventive Medicine and Public Health, School of Medicine, Keio University, Tokyo, Japan – sequence: 11 givenname: Koichi surname: Kobayashi fullname: Kobayashi, Koichi organization: Department of Surgery, Division of General Thoracic Surgery, School of Medicine, Keio University, Tokyo, Japan – sequence: 12 givenname: Michiie surname: Sakamoto fullname: Sakamoto, Michiie email: msakamot@sc.itc.keio.ac.jp organization: Department of Pathology, School of Medicine, Keio University, Tokyo, Japan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18516041$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | 2008 United States & Canadian Academy of Pathology United States and Canadian Academy of Pathology, Inc. 2008 Copyright Nature Publishing Group Aug 2008 |
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Keywords | histopathology micropapillary pattern electron microscopy immunohistochemistry prognosis lung adenocarcinoma |
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A distinct histologic variant with biologic significance publication-title: Am J Surg Pathol doi: 10.1097/00000478-200403000-00004 – volume: 42 start-page: 51 year: 2003 end-page: 57 ident: CR10 article-title: Impact of tumor size on survival in stageIA non-small cell lung cancer: a case for subdividing stageIA disease publication-title: Lung Cancer doi: 10.1016/S0169-5002(03)00285-X – volume: 47 start-page: 479 year: 2005 end-page: 484 ident: CR14 article-title: Primary invasive micropapillary carcinoma of the colon publication-title: Histopathology doi: 10.1111/j.1365-2559.2005.02241.x – volume: 25 start-page: 520 year: 2004 end-page: 522 ident: CR9 article-title: Carcinoembryonic antigen as a predictive factor for postoperative tumor relapse in early-stage lung adenocarcinoma publication-title: Eur J Cardiothorac Surg doi: 10.1016/j.ejcts.2004.01.029 – volume: 45 start-page: 8 year: 2003 end-page: 17 ident: CR6 article-title: Classification, staging and prognosis of lung cancer publication-title: Eur J Radiol doi: 10.1016/S0720-048X(02)00287-5 – volume: 20 start-page: 638 year: 2007 end-page: 647 ident: CR20 article-title: A micropapillary pattern is predictive of a poor prognosis in lung adenocarcinoma, and reduced surfactant apoprotein A expression in the micropapillary pattern is an excellent indicator of a poor prognosis publication-title: Mod Pathol doi: 10.1038/modpathol.3800780 – volume: 56 start-page: 10 year: 2006 end-page: 30 ident: CR2 article-title: Cancer statistics publication-title: CA Cancer J Clin doi: 10.3322/canjclin.56.2.106 – volume: 190 start-page: 668 year: 1994 end-page: 674 ident: CR13 article-title: Invasive micropapillary carcinoma of the breast. 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A distinct histologic variant with biologic significance publication-title: Am J Surg Pathol doi: 10.1097/00000478-200403000-00004 – volume: 123 start-page: 21S issue: 1 Suppl year: 2003 ident: 10.1038/modpathol.2008.79_bib1 article-title: Epidemiology of lung cancer publication-title: Chest doi: 10.1378/chest.123.1_suppl.21S – volume: 112 start-page: 391 year: 1999 ident: 10.1038/modpathol.2008.79_bib11 article-title: Prognostic factors in T1 N0 M0 adenocarcinomas and bronchioloalveolar carcinomas of the lung publication-title: Am J Clin Pathol doi: 10.1093/ajcp/112.3.391 – volume: 16 start-page: 1139 year: 2006 ident: 10.1038/modpathol.2008.79_bib22 article-title: Loss of cell polarity drives tumor growth and invasion through JNK activation in Drosophila publication-title: Curr Biol doi: 10.1016/j.cub.2006.04.042 – volume: 47 start-page: 479 year: 2005 ident: 10.1038/modpathol.2008.79_bib14 article-title: Primary invasive micropapillary carcinoma of the colon publication-title: Histopathology doi: 10.1111/j.1365-2559.2005.02241.x – volume: 124 start-page: 619 year: 1994 ident: 10.1038/modpathol.2008.79_bib23 article-title: Disruption of epithelial cell-matrix interactions induces apoptosis publication-title: J Cell Biol doi: 10.1083/jcb.124.4.619 – volume: 46 start-page: 677 year: 2005 ident: 10.1038/modpathol.2008.79_bib21 article-title: Micropapillary pattern: a distinct pathological marker to subclassify tumours with a significantly poor prognosis within small peripheral lung adenocarcinoma (≤20 mm) with mixed bronchioloalveolar and invasive subtypes (Noguchi’s type C tumours) publication-title: Histopathology doi: 10.1111/j.1365-2559.2005.02126.x – volume: 49 start-page: 63 year: 2005 ident: 10.1038/modpathol.2008.79_bib8 article-title: Smoking history before surgery and prognosis in patients with stageIA non-small-cell lung cancer-a multicenter study publication-title: Lung Cancer doi: 10.1016/j.lungcan.2004.12.006 – volume: 26 start-page: 358 year: 2002 ident: 10.1038/modpathol.2008.79_bib18 article-title: Micropapillary component in lung adenocarcinoma: a distinctive histologic feature with possible prognostic significance publication-title: Am J Surg Patho doi: 10.1097/00000478-200203000-00010 – volume: 20 start-page: 638 year: 2007 ident: 10.1038/modpathol.2008.79_bib20 article-title: A micropapillary pattern is predictive of a poor prognosis in lung adenocarcinoma, and reduced surfactant apoprotein A expression in the micropapillary pattern is an excellent indicator of a poor prognosis publication-title: Mod Pathol doi: 10.1038/modpathol.3800780 – volume: 9 start-page: 701 year: 1997 ident: 10.1038/modpathol.2008.79_bib24 article-title: Integrins and anoikis publication-title: Cur Opin Cell Biol doi: 10.1016/S0955-0674(97)80124-X – volume: 50 start-page: 227 year: 2005 ident: 10.1038/modpathol.2008.79_bib7 article-title: Prognosis of 6644 resected non-small cell lung cancers in Japan: a Japanese Lung Cancer Registry Study publication-title: Lung Cancer doi: 10.1016/j.lungcan.2005.05.021 |
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SubjectTerms | Adenocarcinoma, Papillary - chemistry Adenocarcinoma, Papillary - mortality Adenocarcinoma, Papillary - pathology Adult Aged Aged, 80 and over Basement Membrane - ultrastructure beta Catenin - analysis Biomarkers, Tumor - analysis Cadherins - analysis Connective tissue Disease-Free Survival electron microscopy Female Health care Histopathology Humans Immunoenzyme Techniques immunohistochemistry Ki-67 Antigen - analysis Laboratory Medicine Laminin - analysis lung adenocarcinoma Lung cancer Lung Neoplasms - chemistry Lung Neoplasms - mortality Lung Neoplasms - pathology Lymph Nodes - pathology Lymphatic system Male Medical prognosis Medicine Medicine & Public Health Metastasis micropapillary pattern Microscopy Middle Aged Neoplasm Staging original-article Pathology Patients prognosis Survival analysis Survival Rate Thoracic surgery |
Title | Histopathological features and prognostic significance of the micropapillary pattern in lung adenocarcinoma |
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