Clinical Evaluation
Abnormal bleeding or another concern may lead to examination, transvaginal ultrasound, hysteroscopy, or additional evaluation.
Get a clearer explanation of the diagnosis, tumor type, grade, myometrial invasion, cervical stromal involvement, lymphatic or vascular invasion, margins, lymph nodes, molecular classification, and additional findings documented in your uterine pathology report.
This educational consultation explains your existing written pathology report. It does not provide a new diagnosis, written report, official document, treatment plan, or replacement for your treating clinicians.
Uterine cancer can arise from the endometrial lining or from other uterine tissues. Endometrial carcinoma is usually diagnosed by directly sampling the endometrium, while uterine sarcomas and other less common tumors follow different diagnostic and reporting pathways.
Abnormal bleeding or another concern may lead to examination, transvaginal ultrasound, hysteroscopy, or additional evaluation.
An endometrial biopsy, curettage, or hysteroscopic sample collects tissue so the lining can be examined microscopically.
The report may identify atypical hyperplasia or EIN, endometrial carcinoma, uterine sarcoma, or another diagnosis and specify the tumor type.
If surgery is performed, the larger specimen may document myometrial invasion, cervical involvement, other sites, margins, and lymph nodes.
A biopsy or curettage can establish a diagnosis from sampled tissue. A hysterectomy examines the entire uterus and may provide information about anatomic extent that was not available in the initial sample.
A limited sample may diagnose a precursor lesion or tumor and provide an initial classification.
A hysterectomy specimen may provide a more complete assessment of endometrial carcinoma and its anatomic extent.
The information available depends on the tumor family and specimen. An endometrial biopsy, curettage, hysterectomy, lymph-node specimen, and uterine sarcoma report do not provide the same set of findings.
Endometrial carcinoma, carcinosarcoma, uterine sarcoma, cervical carcinoma involving the uterus, and metastatic disease require different diagnostic and staging frameworks.
The report may identify endometrioid carcinoma, serous carcinoma, clear cell carcinoma, carcinosarcoma, or another tumor type. Uterine sarcomas are classified separately.
Grade describes microscopic features and is reported differently according to tumor type. Endometrioid carcinomas commonly use FIGO grades 1 through 3.
A hysterectomy report may document the greatest gross or microscopic dimension when a measurable tumor is present.
The report may state whether carcinoma invades the uterine muscle and whether invasion involves less than half or at least half of the myometrial thickness.
Invasion into the connective tissue of the cervix is different from tumor involving endocervical glands alone and may affect the pT category.
The report may state whether tumor is present in lymphatic channels or blood vessels and may quantify the number of involved spaces.
Margins are reported when applicable, particularly when carcinoma involves the cervix, parametrium, paracervical tissue, or a relevant specimen edge.
When nodes are submitted, the report may distinguish isolated tumor cells, micrometastases, and macrometastases and identify pelvic or para-aortic involvement.
Review the terminology, key measurements, specimen limitations, invasion findings, and pending results in your existing uterine pathology report during a secure virtual consultation.
For endometrial carcinoma, pT categories reflect depth of invasion into the uterine muscle, cervical stromal invasion, and involvement of specified local or regional structures. Molecular and FIGO classifications may add information beyond the anatomic pT category.
pT1a includes tumor limited to the endometrium or invading less than half of the myometrium. pT1b indicates invasion of half or more.
pT2 requires invasion of cervical stromal connective tissue. Endocervical glandular involvement alone is not classified as pT2.
Complete staging may also use lymph-node findings, distant disease assessment, imaging, operative findings, histologic type, LVSI, molecular results, and treating-team evaluation.
A hysterectomy report may document additional findings considered alongside tumor type, grade, myometrial invasion, molecular classification, lymph nodes, imaging, and other clinical information.
The report may distinguish no invasion, focal involvement of four or fewer spaces, and substantial involvement of five or more spaces on one slide.
The report may address involvement of the uterine surface, ovaries, or fallopian tubes when these tissues are submitted.
Vagina, parametrium, pelvic tissues, bladder or bowel mucosa, omentum, peritoneum, and distant sites are documented when present and sampled.
Cytology may be reported separately. A positive washing result is recorded but does not by itself change the endometrial cancer stage.
Atypical hyperplasia or endometrioid intraepithelial neoplasia, adenomyosis, leiomyomas, polyps, treatment-related changes, or other findings may be documented separately from the carcinoma.
Molecular classification can add information to the histologic diagnosis. Results may appear in the main report, an addendum, or separate molecular and genetics documents.
MMR immunohistochemistry or MSI testing may help classify the tumor. Loss of an MMR protein may lead to additional laboratory or genetics evaluation.
The p53 staining pattern may contribute to molecular classification when interpreted with tumor morphology and other studies.
POLE sequencing and selected tests such as ER, PR, or HER2 may be ordered according to the tumor type and clinical setting and may be reported separately.
Get a patient-friendly explanation of studies already documented in your reports and identify which findings may still be pending or reported separately.
A uterine pathology report may answer many important questions, but it may not provide the complete clinical picture on its own.
The diagnosis, tumor type, grade, myometrial invasion, cervical involvement, LVSI, margins, lymph nodes, and other submitted-site findings may be documented when the specimen allows.
MMR, MSI, p53, POLE, selected biomarkers, outside consultation, later surgical specimens, or germline genetic testing may still be pending or separately reported.
Complete staging and treatment decisions may also require imaging, operative findings, distant-disease assessment, health history, and evaluation by the treating care team.
A pathology report consultation helps you understand terminology and findings already documented, so you can approach conversations with your treating team with greater context and more focused questions.
Submit the pathology report and relevant records requested for the consultation.
Discuss the report during a private virtual appointment and ask questions about the documented findings.
Better understand the terminology and prepare questions to discuss with your treating care team.
A report explanation and a formal microscopic second opinion are different services. Clear boundaries help you choose the appropriate option.
The right option depends on whether you need help understanding written results or an independent review of pathology slides, tissue, or digital images.
These answers provide general educational information. Individual reports vary according to tumor family, specimen, procedure, prior treatment, molecular testing, and wider clinical situation.
Endometrial cancer begins in the uterine lining and is the most common uterine cancer. “Uterine cancer” is broader and can also include tumors arising from uterine muscle or connective tissue, such as uterine sarcomas.
A biopsy or curettage samples part of the endometrium and may establish the diagnosis and initial grade. A hysterectomy examines the uterus and may document myometrial invasion, cervical stromal involvement, other submitted tissues, margins, and lymph nodes.
No. Grade describes microscopic tumor features, while stage describes anatomic extent and may incorporate additional information. The applicable grading and staging systems depend on the tumor type.
Myometrial invasion means carcinoma has extended from the endometrial lining into the uterine muscle. The report may state whether invasion is absent, involves less than half, or involves at least half of the myometrial thickness.
It means endometrial carcinoma has invaded the supportive connective tissue of the cervix. This differs from involvement of endocervical glands alone, which does not qualify as pT2.
It means tumor is identified within lymphatic channels or blood vessels. The report may quantify the involved spaces, and the finding is interpreted with tumor type, grade, depth of invasion, nodes, and stage.
These terms describe molecular groups used in endometrial carcinoma classification. They are determined through combinations of sequencing and immunohistochemistry and should be interpreted with the histologic diagnosis and wider case.
A formal second opinion may be appropriate when findings are complex, uncertain, unexpected, or when independent examination of the original slides or tissue could provide additional value.
Meet online with a pathologist who can explain the terminology, key findings, measurements, specimen limitations, molecular studies, and questions raised by your existing report.
Educational support only. This service does not replace your treating physician, gynecologist, gynecologic oncologist, surgeon, radiologist, genetic counselor, or medical care team.