Literature DB >> 23606697

Intranodal hemorrhagic spindle cell tumor with amianthoid fibers - report of a case with emphasis to mast cell reaction and d2-40 expression.

Anca Maria Cimpean1, Marius Raica.   

Abstract

AIM: Intranodal palisaded myofibroblastoma (IPM) is a rare benign mesenchymal tumor restricted to the lymph nodes. Here, we report the case of a 44-year-old male patient with an IPM confined to the left laterocervical area. CASE REPORT: After an accurate microscopic evaluation of morphological and histochemical stains, immunohistochemistry was performed for vimentin, smooth muscle actin vascular markers, S100 protein, D2-40, Ki67, lymphoid and melanoma markers, keratin and desmin on sections obtained from a paraffin-embedded surgical biopsy.
RESULTS: Spindle cell proliferation was positive for vimentin, smooth muscle cell actin and D2-40 and negative for the other markers. Low proliferative index, assessed by Ki67, was found. Based on morphological and immunohistochemical findings we diagnosed this case as intranodal palisaded myofibroblastoma and we highlighted a D2-40 expression in the tumor spindle cells. The presence of mast cells and their particular distribution inside the tumor are also, together with D2-40 expression, original findings of this study. No therapy was recommended after surgical and histopathological evaluation. The evolution of the patient was favorable with no other relapse following surgical removal of the lymphadenopathy. He has a normal life and no other changes of clinical and biological parameters were registered.
CONCLUSION: To the best of our knowledge, this is the first report regarding a D2-40-positive reaction in the spindle cells of intranodal palisaded myofibroblastoma. Thus, D2-40 could be added to the panel of antibodies used for immunohistochemical diagnosis of such types of tumors.

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Year:  2013        PMID: 23606697

Source DB:  PubMed          Journal:  In Vivo        ISSN: 0258-851X            Impact factor:   2.155


  3 in total

1.  Intranodal palisaded myofibroblastoma: another mesenchymal neoplasm with CTNNB1 (β-catenin gene) mutations: clinicopathologic, immunohistochemical, and molecular genetic study of 18 cases.

Authors:  William B Laskin; Jerzy P Lasota; John F Fetsch; Anna Felisiak-Golabek; Zeng-Feng Wang; Markku Miettinen
Journal:  Am J Surg Pathol       Date:  2015-02       Impact factor: 6.394

2.  Axillary intranodal palisaded myofibroblastoma: report of a case associated with chronic mastitis.

Authors:  Antonio D'Antonio; Maria Addesso; Paolo Amico; Filippo Fragetta
Journal:  BMJ Case Rep       Date:  2014-10-16

3.  Intranodal palisaded myofibroblastoma expressing DOG1: focusing on the potential diagnostic pitfalls.

Authors:  Andreas Kontosis; Evripidis Valanikas; Theodosis Papavramidis; Triantafyllia Koletsa
Journal:  Rom J Morphol Embryol       Date:  2021 Jul-Sep       Impact factor: 0.833

  3 in total

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