Ovarian fibrothecoma

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ORPHA:314478D27
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What is Ovarian fibrothecoma?

Ovarian fibrothecoma is a rare, usually benign (non-cancerous) tumor that grows in the ovary. It belongs to a group of tumors called sex cord-stromal tumors, which develop from the connective tissue cells that support the ovary and produce hormones. The name "fibrothecoma" reflects that the tumor contains a mix of two cell types: fibroma cells (which make fibrous tissue) and thecoma cells (which can produce hormones like estrogen). These tumors are sometimes also called ovarian fibroma-thecoma or simply fibrothecoma. Many women with ovarian fibrothecoma have no symptoms at all, and the tumor is found by chance during imaging or surgery for another reason. When symptoms do occur, they may include pelvic pain or pressure, a feeling of fullness in the abdomen, abnormal vaginal bleeding, or bloating. In some cases, the tumor produces excess estrogen, which can cause irregular periods, postmenopausal bleeding, or thickening of the uterine lining (endometrial hyperplasia). A rare but notable complication is Meigs syndrome, where the tumor causes fluid to build up in the abdomen (ascites) and around the lungs (pleural effusion). The main treatment for ovarian fibrothecoma is surgery to remove the tumor. In younger women who wish to preserve fertility, only the affected ovary may be removed. In older or postmenopausal women, removal of both ovaries and the uterus may be recommended. Because these tumors are almost always benign, the outlook after surgery is generally excellent, and recurrence is very rare.

Key symptoms:

Pelvic pain or discomfortAbdominal bloating or swellingFeeling of fullness or pressure in the lower bellyAbnormal vaginal bleedingPostmenopausal bleedingIrregular menstrual periodsFluid buildup in the abdomen (ascites)Fluid around the lungs causing shortness of breathUnexplained weight gain in the abdomenPain during intercourseUrinary frequency from pressure on the bladderConstipation from pressure on the bowel

Clinical phenotype terms (15)— hover any for plain English
  • Abnormality of the ovaryHP:0000137
  • PeritonitisHP:0002586
  • Abnormal circulating hormone concentrationHP:0003117
  • Diffuse leiomyomatosisHP:0006756
  • Gonadal calcificationHP:0008703
  • Ovarian fibromaHP:0010618
  • Increased serum testosterone levelHP:0030088
  • Abnormal endometrium morphologyHP:0030126
  • FibrosarcomaHP:0100244
  • MetrorrhagiaHP:0100608
Inheritance
Sporadic
Usually appears on its own, not inherited from a parent
Age of Onset
Adult
Begins in adulthood (age 18 or older)
Orphanet ↗NORD ↗

Treatments

Source: openFDA + DailyMed · NDA / BLA labels with structured indications · refreshed weekly

No FDA-approved treatments are currently listed for Ovarian fibrothecoma.

View clinical trials →

Source: ClinicalTrials.gov · synced daily · phases, status, and PI names normalized at ingest

No actively recruiting trials found for Ovarian fibrothecoma at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Ovarian fibrothecoma community →

Source: NPI Registry + PubMed · trial PI roles cross-referenced with ClinicalTrials.gov · ranked by match score (publications + PI activity + community signal)

No specialists are currently listed for Ovarian fibrothecoma.

View NORD Rare Disease Centers ↗Undiagnosed Disease Network ↗

Treatment Centers

8 centers

Source: NORD Rare Disease Centers + NIH Undiagnosed Diseases Network (UDN) · centers verified active within last 12 months

🏨 Children's

Children's Hospital Colorado Rare Disease Program

Children's Hospital Colorado

📍 Aurora, CO

👤 Boston Children's Hospital Rare Disease Program

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Boston Children's Hospital Rare Disease Program

Boston Children's Hospital

📍 Boston, MA

👤 Boston Children's Hospital Rare Disease Program

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

🏨 Children's

Ann & Robert H. Lurie Children's Hospital Genetics

Lurie Children's Hospital

📍 Chicago, IL

👤 Boston Children's Hospital Rare Disease Program

🏥 NORD

Cincinnati Children's Hospital Medical Center

Cincinnati Children's

📍 Cincinnati, OH

👤 Boston Children's Hospital Rare Disease Program

🏨 Children's

Nationwide Children's Hospital Rare Disease Center

Nationwide Children's Hospital

📍 Columbus, OH

👤 Boston Children's Hospital Rare Disease Program

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

Travel Grants

No travel grants are currently matched to Ovarian fibrothecoma.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Ovarian fibrothecoma

Source: PubMed + NIH RePORTER + openFDA + clinical-journal RSS · last 30 days · disease-tagged at ingest by AI extraction with human QC

No recent news articles for Ovarian fibrothecoma.

Follow this condition to be notified when news becomes available.

Caregiver Resources

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Questions for your doctor

Bring these to your next appointment

  • Q1.Is my tumor benign, and how can you be sure it is not cancerous?,What type of surgery do you recommend, and can my ovary or fertility be preserved?,Is my tumor producing hormones, and could that be causing my symptoms?,Do I have Meigs syndrome, and will the fluid go away after surgery?,What is the chance that this tumor could come back after removal?,Will I need hormone replacement therapy after surgery?,How often should I have follow-up visits and imaging after treatment?

Common questions about Ovarian fibrothecoma

What is Ovarian fibrothecoma?

Ovarian fibrothecoma is a rare, usually benign (non-cancerous) tumor that grows in the ovary. It belongs to a group of tumors called sex cord-stromal tumors, which develop from the connective tissue cells that support the ovary and produce hormones. The name "fibrothecoma" reflects that the tumor contains a mix of two cell types: fibroma cells (which make fibrous tissue) and thecoma cells (which can produce hormones like estrogen). These tumors are sometimes also called ovarian fibroma-thecoma or simply fibrothecoma. Many women with ovarian fibrothecoma have no symptoms at all, and the tumor

How is Ovarian fibrothecoma inherited?

Ovarian fibrothecoma follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Ovarian fibrothecoma typically begin?

Typical onset of Ovarian fibrothecoma is adult. Age of onset can vary across affected individuals.

Frequently asked questions about Ovarian fibrothecoma

Auto-generated from canonical disease facts (Orphanet, OMIM, ClinicalTrials.gov, openFDA, NPPES). Not a substitute for clinical guidance.

  1. What is Ovarian fibrothecoma?

    Ovarian fibrothecoma is a rare disease catalogued in international rare-disease ontologies (Orphanet ORPHA:314478). It is typically inherited as sporadic. Age of onset is generally adult. For verified primary sources, see the UniteRare Ovarian fibrothecoma page.

  2. How is Ovarian fibrothecoma inherited?

    Ovarian fibrothecoma follows sporadic inheritance. Genetic counseling is recommended for affected families to understand recurrence risk in offspring and the likelihood of unaffected siblings being carriers. Variants in the underlying gene(s) may be identified via clinical genetic testing.

  3. Are there FDA-approved treatments for Ovarian fibrothecoma?

    Approved treatments for Ovarian fibrothecoma are tracked from openFDA and DailyMed primary sources. Many rare diseases have no specific FDA-approved therapy; for those, supportive care and management of complications form the basis of clinical care. Orphan-drug-designation status is noted where applicable.

  4. Are there clinical trials for Ovarian fibrothecoma?

    Active clinical trials for Ovarian fibrothecoma are tracked daily from ClinicalTrials.gov. Trial availability changes frequently; check the UniteRare trial listings for the current count and recruitment status. Sponsors of rare-disease research often welcome inquiries even when a trial is not actively recruiting at a given moment.

  5. How do I find a specialist for Ovarian fibrothecoma?

    Verified Ovarian fibrothecoma specialists are identified through ClinicalTrials.gov principal-investigator records, peer-reviewed publication authorship (via PubMed), and the NPPES NPI registry. NORD-designated Centers of Excellence and NIH-affiliated rare-disease clinics are also tracked. UniteRare's specialist directory is updated continuously as new evidence becomes available.

See full Ovarian fibrothecoma page for complete clinical details, sources, and verified-specialist listings.

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