Mucinous cystadenocarcinoma differential diagnosis: Difference between revisions

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Revision as of 20:58, 23 February 2016

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

@@ Line 2: / Line 2: @@
 {{Mucinous cystadenocarcinoma}}
 {{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==
 {{reflist|2}}