D. Zagzag et al., DEMYELINATING DISEASE VERSUS TUMOR IN SURGICAL NEUROPATHOLOGY - CLUESTO A CORRECT PATHOLOGICAL DIAGNOSIS, The American journal of surgical pathology, 17(6), 1993, pp. 537-545
Clinical presentations as well as radiological and histopathological f
indings in biopsies from patients with multiple sclerosis (MS) or othe
r demyelinating disorders of the central nervous system are sometimes
misleading, resulting in an erroneous diagnosis of brain or spinal cor
d tumor. We report 17 patients who presented with symptoms mimicking t
hose of brain (14 cases) or spinal cord (three cases) tumors. Computer
ized tomography or magnetic resonance imaging studies or both were int
erpreted as consistent with a tumor in each case. All patients underwe
nt surgery, and all 17 pathological specimens were eventually diagnose
d as showing demyelinating disease, usually consistent with MS. In eac
h case we examined a variety of histological features and immunohistoc
hemical studies and addressed their relative importance in considering
the diagnosis of MS. All cases showed perivascular lymphocytic inflam
mation with variable amounts of macrophage infiltration, necrosis, and
edema. The hypercellularity of the lesions and the presence of atypic
al reactive astrocytes with mitotic figures were the disturbing featur
es that might have led to the erroneous diagnosis of an astrocytic neo
plasm. Immunohistochemistry for astrocytic (glial fibrillary acidic pr
otein) and macrophage (HAM-56) markers are helpful in evaluating biops
ies. Our results emphasize the need to perform special stains (i.e., f
or myelin and axons) that demonstrate myelin loss and relative preserv
ation of axons and allow a correct diagnosis.