Jh. Shanks et al., Mesotheliomas with deciduoid morphology - A morphologic spectrum and a variant not confined to young females, AM J SURG P, 24(2), 2000, pp. 285-294
Citations number
32
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Deciduoid mesotheliomas are rare with only four previously reported cases,
all affecting the peritoneum of young females. We describe another six case
s (three men and three women; age range 52-65 yrs, median 55 yrs; five peri
toneal and one pleural). Three patients had an occupational history of asbe
stos exposure. The deciduoid appearance predominated in four cases, whereas
in two it represented a minor component within conventional tubulopapillar
y epithelioid mesothelioma. All tumors were strongly cytokeratin-positive (
including CK5/6) and all showed at least focal staining for thrombomodulin,
HBME-1, and calretinin. All were negative for epithelial mucin (D/PAS), CE
A, BerEP4, LeuM1 (CD15), CD21, CD35, and S100 protein, Five of six cases (8
3%) were vimentin-positive and two (33%) were focally positive for alpha-sm
ooth muscle actin. A differential diagnosis of gastrointestinal autonomic n
erve tumor (GANT) had been initially considered from the morphology of one
case, and we found positivity for some of the "neuronal" markers described
in GANTs. This prompted us to apply such a panel to the other five tumors,
accepting that the cytokeratin positivity encountered in all of our cases w
ould exclude GANT. All cases of deciduoid mesothelioma (100%) were positive
for PGP 9.5 and NSE and four of six (66%) were positive for NKI/C3. Weak f
ocal staining (<5% cells) for syn aptophysin was seen in two of six tumors.
All cases were chromogranin-negative. All cases examined by electron micro
scopy showed desmosomes and smooth microvilli without rootlets but no neurc
endocrine granules. In conclusion, a de ciduoid morphology appears to be pa
rt of the histopathologic spectrum encountered in epithelioid mesothelioma.
This variant is not confined to female patients and occurs over a wider ag
e range than previously recognized. The overlapping immunophenotype with GA
NTs illustrates that caution should be exercised when interpreting positivi
ty for "neuronal" markers in this context. An immunohistochemical panel tha
t includes cytokeratins should always be used.