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      Structure and Distribution of an Unrecognized Interstitium in Human Tissues

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          Abstract

          Confocal laser endomicroscopy (pCLE) provides real-time histologic imaging of human tissues at a depth of 60–70 μm during endoscopy. pCLE of the extrahepatic bile duct after fluorescein injection demonstrated a reticular pattern within fluorescein-filled sinuses that had no known anatomical correlate. Freezing biopsy tissue before fixation preserved the anatomy of this structure, demonstrating that it is part of the submucosa and a previously unappreciated fluid-filled interstitial space, draining to lymph nodes and supported by a complex network of thick collagen bundles. These bundles are intermittently lined on one side by fibroblast-like cells that stain with endothelial markers and vimentin, although there is a highly unusual and extensive unlined interface between the matrix proteins of the bundles and the surrounding fluid. We observed similar structures in numerous tissues that are subject to intermittent or rhythmic compression, including the submucosae of the entire gastrointestinal tract and urinary bladder, the dermis, the peri-bronchial and peri-arterial soft tissues, and fascia. These anatomic structures may be important in cancer metastasis, edema, fibrosis, and mechanical functioning of many or all tissues and organs. In sum, we describe the anatomy and histology of a previously unrecognized, though widespread, macroscopic, fluid-filled space within and between tissues, a novel expansion and specification of the concept of the human interstitium.

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          Most cited references18

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          Keloids and Hypertrophic Scars: Pathophysiology, Classification, and Treatment.

          Keloid and hypertrophic scars represent an aberrant response to the wound healing process. These scars are characterized by dysregulated growth with excessive collagen formation, and can be cosmetically and functionally disruptive to patients.
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            Clinical usefulness of variable-frequency ultrasound in localized lesions of the skin.

            High variable-frequency ultrasound is a recently available technique capable of clearly defining skin layers and deeper structures that also provides local perfusion patterns obtained in real time. The aim of the study was to assess the performance of variable-frequency ultrasound in the evaluation of skin lesions. We performed a retrospective study of 4338 skin ultrasound examinations in predominantly localized skin lesions, and in a group of 130 healthy controls. We determined ultrasound sensitivity, specificity, and statistical level of certainty, and compared ultrasound diagnoses with clinical diagnoses. Referring diagnosis was correct in 73% of the lesions, and addition of ultrasound increased correctness to 97% (P < .001 for the difference). Ultrasound overall sensitivity was 99%, specificity was 100%, and statistical diagnostic certainty was 99% Ultrasound in its current version cannot detect lesions that are epidermal only or that measure less than 0.1 mm in depth. Ultrasound is a reliable adjuvant for the accurate and precise diagnosis of skin lesions. Copyright (c) 2009 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved.
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              Preclinical intravital microscopy of the tumour-stroma interface: invasion, metastasis, and therapy response.

              Key steps of cancer progression and therapy response depend upon interactions between cancer cells with the reactive tumour microenvironment. Intravital microscopy enables multi-modal and multi-scale monitoring of cancer progression as a dynamic step-wise process within anatomic and functional niches provided by the microenvironment. These niches deliver cell-derived and matrix-derived signals that enable cell subsets or single cancer cells to survive, migrate, grow, undergo dormancy, and escape immune surveillance. Beyond basic research, intravital microscopy has reached preclinical application to identify mechanisms of tumour-stroma interactions and outcome. We here summarise how n-dimensional 'dynamic histopathology' of tumours by intravital microscopy shapes mechanistic insight into cell-cell and cell-tissue interactions that underlie single-cell and collective cancer invasion, metastatic seeding at distant sites, immune evasion, and therapy responses. Copyright © 2013 Elsevier Ltd. All rights reserved.
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                Author and article information

                Contributors
                neil.theise@nyumc.org
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                27 March 2018
                27 March 2018
                2018
                : 8
                : 4947
                Affiliations
                [1 ]ISNI 0000 0001 0670 2351, GRID grid.59734.3c, Department of Medicine, , Division of Digestive Diseases, Mount Sinai Beth Israel Medical Center, Icahn School of Medicine at Mount Sinai, New York, ; New York, 10003 USA
                [2 ]Department of Medicine, Division of Gastroenterology, Zucker School of Medicine at Hofstra/Northwell, 500 Hofstra Blvd, Hempstead, NY 11549 USA
                [3 ]ISNI 0000 0004 1936 8972, GRID grid.25879.31, Department of Medicine, , Division of Gastroenterology, Perelman School of Medicine, University of Pennsylvania, ; Philadelphia, Pennsylvania 19104 USA
                [4 ]ISNI 0000 0004 1936 8972, GRID grid.25879.31, Department of Bioengineering and Center for Engineering MechanoBiology, , School of Engineering and Applied Sciences, University of Pennsylvania, ; Philadelphia, Pennsylvania 19104 USA
                [5 ]ISNI 0000 0001 0670 2351, GRID grid.59734.3c, Department of Pathology, , Mount Sinai Beth Israel Medical Center, Icahn School of Medicine at Mount Sinai, New York, ; New York, 10003 USA
                [6 ]ISNI 0000 0004 1936 8753, GRID grid.137628.9, Department of Pathology, , New York University School of Medicine, New York, ; New York, 10016 USA
                [7 ]ISNI 0000 0001 0670 2351, GRID grid.59734.3c, Department of Surgery, , Mount Sinai Beth Israel Medical Center, Icahn School of Medicine at Mount Sinai, New York, ; New York, 10003 USA
                [8 ]ISNI 0000 0000 8499 1112, GRID grid.413734.6, The Center for Advanced Digestive Care, , Weill Cornell Medicine, New York Presbyterian Hospital, 1305 York Avenue, 4th Floor, New York, ; New York, 10021 USA
                Article
                23062
                10.1038/s41598-018-23062-6
                5869738
                29588511
                731f262c-840b-46a9-936f-7edc0a30a617
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 18 May 2017
                : 6 March 2018
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