Mucinous cystadenocarcinoma differential diagnosis: Difference between revisions

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{{Mucinous cystadenocarcinoma}}
{{Mucinous cystadenocarcinoma}}
{{CMG}}; {{AE}} {{Ammu}}
{{CMG}}; {{AE}} {{Ammu}}
==Overview==


==Pathogenesis==
==Genetics==
==Associated Conditions==
==Gross Pathology==
Features:
Multiloculated.
Sticky, gelatinous fluid (glycoprotein).
+/-Necrosis.
Typically unilateral.[3]
==Microscopic Pathology==
Features:
Mucinous differentiation.
Tall columnar cells in glands with apical mucin.
May have an endocervical-like or intestinal-like appearance - see subtypes.
Invasive morphology - one of the following:
Back-to-back glands/confluent growth pattern.
Desmoplastic stromal response.
Cribriforming of glands.
Malignant characteristics:
+/-Nuclear atypia.
+/-Necrosis.
No cilia.
==References==
==References==
{{reflist|2}}
{{reflist|2}}

Revision as of 20:58, 23 February 2016

Mucinous cystadenocarcinoma Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]

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