Overview of Tumors
Certain benign tumors, like teratomas, are often self-limiting if composed entirely of mature tissues.
There are different types of teratomas that primarily occur in the ovaries, with mature solid and cystic teratomas being the most common types.
Mature Solid Teratoma
Predominantly solid in gross appearance, with small cystic areas present.
Composed entirely of adult tissues from all three germ layers.
Requires extensive sampling to differentiate from grade 1 immature teratoma; some refer to it as "grade 0" immature teratoma.
Primarily occurs in young women (second decade of life) and has an excellent prognosis, including cases with peritoneal implants.
Mature Cystic Teratoma
Accounts for about 20% of all ovarian neoplasms and is most common in childhood (88% unilateral).
Often manifests symptoms related to mass effects but can lead to complications such as hemolytic anemia, virilization, or paraneoplastic encephalitis, commonly linked to NMDA receptor antibodies.
Grossly multiloculated with cystic content primarily containing keratin, sebum, and hair; may have structures like teeth and even rudimentary human features (fetiform teratomas).
Histologically, it includes variations in tissue types such as epidermis, glial tissue, respiratory tissue, gastrointestinal tract tissue, and thyroid tissue in 10% of cases.
Grading of Immature Teratomas
Grade I: Rare foci of immature neuroepithelial tissue.
Grade II: Occasional immature neuroepithelial foci with mitoses.
Grade III: Few mature tissues, extensive neuroepithelial elements present.
Distinguishing features are necessary to differentiate from teratomas with yolk sac or embryonal carcinoma patterns.
Complications and Changes Related to Teratoma
Peritoneal nodules composed of mature glial and neuronal tissue indicate a benign condition known as gliomatosis peritonei.
Rupture of mature teratomas can lead to foreign body reactions mimicking metastatic cancers.
Somatic-type Tumors in Mature Cystic Teratomas
Rare, occurring in approximately 2% of cases; can exhibit malignant changes like squamous cell carcinoma.
Other possible tumors include carcinoid tumors, adenocarcinoma, and various sarcomas.
Malignant transformations may result in significant chromosomal aberrations.
Epidermoid Cyst and Struma Ovarii
Epidermoid cysts represent a different entity from mature cystic teratomas; may arise from epithelial cell nests but lack skin adnexal components.
Struma ovarii refers to the predominance of thyroid tissue in a teratoma, which may lead to conditions like hyperthyroidism and is distinguishable by immunohistochemical studies.
Carcinoid Tumors
Can occur as metastases or primary tumors in the ovary.
Primary ovarian carcinoids can exhibit aggressive behavior and may develop carcinoid syndrome independent of metastases.
Mucinous types are aggressive and may carry a poor prognosis.
Sex Cord–Stromal Tumors
Make up about 5% of ovarian neoplasms, differentiating in the direction of sex cords and specialized stroma.
Granulosa cell tumors are the most significant subtype, with hormonal implications, variable growth patterns, and specific immunohistochemical markers like inhibin and FOXL2.
Adult type is often linked with hyperestrinism, while juvenile type can occur in younger patients.
Immunohistochemical Markers
Inhibin, FOXL2, SF-1: These markers help identify sex cord-stromal tumors.
Variability in staining may complicate diagnosis, and the absence of immunohistochemical staining does not exclude tumoral presence.
Key Considerations
Thorough sampling and accurate diagnosis are essential due to overlapping characteristics between different tumor types.