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RUNX‐1 and CD44 as markers of resident stem cell derivation in undifferentiated intimal sarcoma of pulmonary artery
Author(s) -
Vasuri Francesco,
Resta Leonardo,
Fittipaldi Silvia,
Malvi Deborah,
Pasquinelli Gianandrea
Publication year - 2012
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1111/j.1365-2559.2012.04241.x
Subject(s) - pathology , calponin , biology , cd31 , cd34 , stem cell , stem cell marker , cd90 , immunohistochemistry , microbiology and biotechnology , medicine
Vasuri F, Resta L, Fittipaldi S, Malvi D & Pasquinelli G
(2012) Histopathology 61, 737–743 RUNX‐1 and CD44 as markers of resident stem cell derivation in undifferentiated intimal sarcoma of pulmonary artery Aims: To report a rare case of undifferentiated intimal sarcoma (UIS) of the pulmonary artery in a 44‐year‐old woman, and to study it by electron microscopy and a novel immunohistochemical (IHC) panel that recognizes markers of endothelial and haematopoietic stemness, in order to extend current knowledge about the histogenesis of this rare neoplasm. Methods and results: Immunohistochemical reactions for CD31, CD34, α‐smooth muscle actin (α‐SMA), caldesmon, calponin, actin, desmin, epithelial membrane antigen, WT1, CD117, Ki67, nestin, RUNX‐1, platelet‐derived growth factor, NG2, CD44, CD90 and CD105 were performed manually or automatically. Neoplastic cells were negative for CD31 and CD34, but positive for calponin, nestin, WT1, CD44, and RUNX‐1. Electron microscopy was performed after osmium tetroxide fixation and staining with lead citrate and uranyl acetate. Ultrastructurally, tumour cells had slightly irregular nuclei, cisternae of rough endoplasmic reticulum, and punctate intercellular junctions. Conclusions: We report a case of pulmonary artery UIS expressing previously unreported markers, i.e. RUNX‐1, nestin, WT1, and CD44, that are commonly seen in different stages of the vascular differentiation hierarchy. These findings, together with the negativity for mature endothelial and smooth muscle markers, raise the question of whether this neoplasm may derive from a vessel wall‐resident stem cell, such as the haemangioblast or an embryonic‐like stem cell.