@article{21639, keywords = {Humans, Immunohistochemistry, Leprosy, Tuberculoid, Microscopy, Electron, Transmission, Nerve Fibers, Peripheral nerves, Schwann Cells}, author = {Antunes S and Medeiros MF and CĂ´rte-Real S and Jardim M and Nery JC and Hacker M and Valentim VC and Amadeu TP and Sarno E}, title = {Microfasciculation: a morphological pattern in leprosy nerve damage.}, abstract = {
AIMS: To study Microfasciculation, a perineurial response found in neuropathies, emphasizing its frequency, detailed morphological characteristics and biological significance in pure neural leprosy (PNL), post-treatment leprosy neuropathy (PTLN) and non-leprosy neuropathies (NLN).
METHODS AND RESULTS: Morphological characteristics of microfascicles were examined via histological staining methods, immunohistochemical expression of neural markers and transmission electronmicroscopy. The detection of microfasciculation in 18 nerve biopsy specimens [12 PNL, six PTLN but not in the NLN group, was associated strongly with perineurial damage and the presence of a multibacillary inflammatory process in the nerves, particularly in the perineurium. Immunoreactivity to anti-S100 protein, anti-neurofilament, anti-nerve growth receptor and anti-myelin basic protein immunoreactivity was found within microfascicles. Ultrastructural examination of three biopsies showed that fibroblast-perineurial cells were devoid of basement membrane despite perineurial-like NGFr immunoreactivity. Morphological evidence demonstrated that multipotent pericytes from inflammation-activated microvessels could be the origin of fibroblast-perineurial cells.
CONCLUSIONS: A microfasciculation pattern was found in 10% of leprosy-affected nerves. The microfascicles were composed predominantly of unmyelinated fibres and denervated Schwann cells (SCs) surrounded by fibroblast-perineurial cells. This pattern was found more frequently in leprosy nerves with acid-fast bacilli (AFB) and perineurial damage while undergoing an inflammatory process. Further experimental studies are necessary to elucidate microfascicle formation.
}, year = {2011}, journal = {Histopathology}, volume = {58}, pages = {304-11}, month = {2011 Jan}, issn = {1365-2559}, doi = {10.1111/j.1365-2559.2011.03749.x}, language = {eng}, }