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Tag Archives: mucinous adenocarcinoma
Endometrial Adenocarcinoma
Endometrial Adenocarcinoma
Endometrioid Adenocarcinoma of Uterus
What are the different variants?
- villoglandular
- adenoma malignum
- secretory (subnuclear vacuolization, resembles POD2)
- ciliated (cilia, differential diagnosis is cilia cell metaplasia)
Histology: thin, long, delicate fronds with pseudostratified endometrium (villoglandular)
- low grade nuclei
Differential diagnosis:
- serous papillary endometrial adenocarcinoma (p53 negative in villoglandular endometrial adenocarcinoma)
- endometrial vs. cervical endometrioid adenocarcinoma:
use the immunohistochemistry panel (vimentin +, CEA -, ER +, HPV -, p16 -)
Serous Adenocarcinoma of Uterus
Histology: short papillae with fibrovascular cores, slit like glands
- high grade nuclei and multiple mitoses
- psammoma bodies
Immunohistochemistry: p53 positive in > 70% of nuclei (differential diagnosis of endometrial)
Clear Cell Adenocarcinoma of Uterus
Histology:
- high grade nuclei
- hobnail cells
SS: PAS positive glycogen in cytoplasm
Mucinous Adenocarcinoma of Uterus
Histology: endocervical-type lining of glands with pseudostratification
- need > 50% differentiation
Special Stains: mucicarmine, Alcian blue
Grading: same as endometrial
Rare Endometrial Cancer Types
Squamous
Mixed
Small cell neuroendocrine carcinoma
- like other small cell carcinoma
Endometrial Adenocarcinoma Genetics
Endometrioid: mutations and MSI in PTEN, k-ras and β-catenin
Non-endometrioid: mutations in p53
Endometrial Adenocarcinoma Invasion
Muscular invasion (deep or associated granulation tissue) vs.
1) Expansion of endometrial-myometrial junction
2) Adenomyosis
Endometrial Adenocarcinoma Treatment
Endometrioid: total abdominal hysterectomy and bilateral salpingo-oophorectomy (TAH-BSO)
{+/- surgical staging (pelvic and para-aortic nodes & peritoneal cytology)}
Serous: TAH-BSO and surgical staging and adjuvant therapy
Posted in Uterus
Tagged adenocarcinoma, adenoma malignum, Ciliated Endometrioid Adenocarcinoma, Clear Cell Adenocarcinoma, Clear Cell Adenocarcinoma of Uterus, Endometrial adenocarcinoma, Endometrial Adenocarcinoma Genetics, Endometrial Adenocarcinoma Invasion, Endometrial Adenocarcinoma Treatment, endometrial cancer, Endometrial Cancer Genetics, endometrial carcinoma, Endometrioid Adenocarcinoma, Endometrioid Adenocarcinoma of Uterus, Endometrioid Cancer, mucinous adenocarcinoma, Mucinous Adenocarcinoma of Uterus, Mucinous cancer, Secretory Endometrioid Adenocarcinoma, Serous Adenocarcinoma, Serous Adenocarcinoma of Uterus, villoglandular
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Hereditary Nonpolyposis Colorectal Cancer Syndrome
Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Syndrome
Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Syndrome, also known as Lynch syndrome, is a rare colorectal syndrome that can lead to cancer of the colon.
Hereditary Nonpolyposis Colorectal Cancer Syndrome Inheritance pattern
- autosomal dominant
- syndromal patients have only one functional allele and cancer occurs through loss of heterozygosity (LOH)
- mutations occur in mismatch repair genes (MLH1, MSH 2, MSH6, PMS 1, PMS 2)
- mutations lead to microsatellite instability which are mostly repeats in intronic regions
What to look for?
- you can look for the loss of the genes themselves
- you can look at particular microsatellite loci and see how many have instability
- 0/5 – stable
- 1/5 – low frequency instability
- 2 or greater/5 – high frequency of instability – MSI-H
- microsatellite instability is NOT specific to HNPCC, as it is seen in 10-15 % of sporadic colorectal carcinomas. Sporadic tumors arise in older patients who lack a family history. The activity of the mismatch repair genes in sporadic tumors is lost through hypermethylation
Diagnostic criteria is through the Amsterdam II criteria
Clinical presentation
- development of multiple cancers at an early age, including cancer of the colon, endometrium, renal pelvis and ureter, small bowel, ovary, brain, hepatobiliary tract and sebaceous tumors
Muir -Torre Syndrome
- sebaceous tumors along with HNPCC type of internal malignancy
Turcot Syndrome
- tumors of the CNS (usually gliobalstomas) and multiple colorectal tumors
Gross Appearance
- predilection for right colon and cecum all the way to the transverse colon
- usually polypoid in appearnace rather than diffuse
Microscopic Appearance
- sporadic tumors have the same features as tumors associated with HNPCC
- proximally located mucinous type of colorectal adenocarcinomas +/- tumor infiltrating lymphocytes
- proximally located, poorly differentiated medullary or undifferentiated colorectal adenocarcinomas – these are well circumscribed and lacking abundant desmoplastic stroma and may contain tumor infiltrating lymphocytes
- adenomas – many have a villous morphology and high grade dysplasia, with rapid progression to carcinoma
Posted in Colon, GI, Syndrome
Tagged , gross, Hereditary Nonpolyposis Colorectal Cancer Syndrome, hnpcc, loss of heterozygosity, lynch syndrome, medullary adenocarcinoma, microsatellite instability, microscopic, mismatch repair genes, mlh, mucinous adenocarcinoma, muir-torre syndrome, multiple cancers, mutations, right colon, Syndrome, turcot syndrome
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