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1.WELL DIFFERENTIATED PAPILLARY
MESOTHELIOMA:
2.LOCALIZED MALIGNANT
MESOTHELIOMA:
3.MULTICYSTIC MESOTHELIOMA:
4.ADENOMATOID
TUMOUR
WELL DIFFERENTIATED PAPILLARY
MESOTHELIOMA:
Well-differentiated
papillary mesothelioma (WDPM) is considered a specific clinico-pathologic entity distinct from
conventional diffuse malignant mesothelioma.
The majority of cases have been reported in the
peritoneum in women of reproductive age with no history of asbestos exposure
and also in the tunica vaginalis of men. Cases have also been reported in
the pleura.
WDPM is often
discovered incidentally during abdominal or pelvic surgery.
The tumour has an
indolent clinical course and with a good prognosis. Occasional cases are
more aggressive and require long term clinical follow-up.
Macroscopic
features:
Multiple grey white nodules usually less than 20mm in
diameter.
Microscopic
features:
Well defined stout
papillary structures with myxoid cores, lined
by bland, flattened, single layer of cuboidal or columnar mesothelial cells.
Subnuclear vacuolation may be noted. Mitotic figures are rarely present. In
some cases there may be limited invasion
of the submesothelial layer. Deep invasion is usually not seen.
Differential
diagnosis:
Reactive mesothelial
hyperplasia (assocciated with inflammation) ;
Serous neoplasia of
peritoneum ( cellular stratification, atypia and mitotic figures) ;
Primary and seconday
adenocarcinoma (mucin histochemistry and immunohistochemistry are useful ) ;
Diffuse mesothelioma
with a prominent tubulopapillary epithelial component (diffuse growth
pattern & cytological atypia).
LOCALIZED MALIGNANT
MESOTHELIOMA:
Localized malignant mesotheliomas are uncommon, sharply circumscribed tumours
of the serosal membranes with the microscopic appearance of diffuse
malignant mesothelioma but without any evidence of diffuse spread.
This lesion should not be confused with localized fibrous tumours as
localized malignant mesothelioma has a more aggressive clinical behaviour.
MULTICYSTIC MESOTHELIOMA:
Multicystic
mesothelioma is a rare form of mesothelioma. It is an extremely rare benign
neoplastic disease with high tendency to recur locally, but no tendency to
malignancy.
There is often
history of previous surgery, pelvic inflammatory disease or endometriosis.
The lesion is not associated with asbestos exposure.
Macroscopic
features:
Single or multiple thin-walled cysts.
Microscopic
features: Cysts are multilocular thin-walled and lined by single layer
of cuboidal mesothelial cells.
Differential
diagnosis: Diffuse malignant mesothelioma with a cystic/angiomatoid
component( multicystic mesothelioma is localized in nature) and cystic
lymphangioma.
Correct diagnosis
of multicystic mesothelioma can be made with histopathologic examination and
always with immunohistochemical and ultrastructural evaluation.
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