Ovarian fibroma

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8Specialists8Treatment centers

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UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
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Overview

Ovarian fibroma is a rare, 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. Ovarian fibromas make up a small percentage of all ovarian tumors, and they are most commonly found in women who are middle-aged or older, typically around or after menopause. These tumors are usually solid, slow-growing, and found on one ovary. Most ovarian fibromas do not produce hormones, so they often grow silently without causing obvious symptoms at first. As the tumor gets larger, women may notice pelvic pain, a feeling of fullness or pressure in the abdomen, or bloating. In some cases, a condition called Meigs syndrome can develop, where fluid builds up around the lungs (pleural effusion) and in the abdomen (ascites), which can cause shortness of breath and abdominal swelling. This can sometimes be mistaken for a sign of cancer, but it resolves once the tumor is removed. The main treatment for ovarian fibroma is surgery. In younger women who wish to preserve fertility, the surgeon may remove only the tumor or the affected ovary. In older women or when the tumor is large, removal of the ovary and sometimes the fallopian tube may be recommended. Because these tumors are benign, the outlook after surgery is generally excellent, and recurrence is rare.

Key symptoms:

Pelvic pain or discomfortAbdominal bloating or swellingFeeling of fullness or pressure in the lower bellyFluid buildup in the abdomen (ascites)Fluid buildup around the lungs causing shortness of breathIrregular menstrual periodsDifficulty breathing when lying flatUnexplained weight gain from fluid retentionConstipation or urinary frequency from pressure on nearby organsA pelvic mass felt during a physical examNo symptoms at all in early stages

Clinical phenotype terms (11)— hover any for plain English
Abnormality of the ovaryHP:0000137PeritonitisHP:0002586Gonadal calcificationHP:0008703Odontogenic keratocysts of the jawHP:0010603Ovarian fibromaHP:0010618Mesenteric cystHP:0030451
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

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

View clinical trials →

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

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

Search ClinicalTrials.gov ↗Join the Ovarian fibroma community →

Specialists

8 foundView all specialists →
RP
Robert Maki, MD, PhD
PHILADELPHIA, PA
Specialist
PI on 8 active trials
SP
Sandip P Patel
Birmingham, Alabama
Specialist

Rare Disease Specialist

PI on 1 active trial
SM
Shivaani Kummar, MD
PORTLAND, OR
Specialist
PI on 5 active trials
MM
Mary L. Keohan, MD
NEW YORK, NY
Specialist
PI on 1 active trial
SP
Sunil Singhal, MD, Ph.D
PHILADELPHIA, PA
Specialist
PI on 1 active trial
MM
Michael Heinrich, MD
Specialist
PI on 1 active trial

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Ovarian fibroma.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Ovarian fibroma

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Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

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Family & Caregiver Grants

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Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Questions for your doctor

Bring these to your next appointment

  • Q1.Is my ovarian fibroma likely to be benign, and how can you be sure it is not cancerous?,What type of surgery do you recommend, and will I be able to have children afterward?,Could this tumor be related to a genetic condition like Gorlin syndrome, and should I have genetic testing?,What are the risks of the surgery, and how long will recovery take?,Is there any chance the tumor could come back after it is removed?,Do I have Meigs syndrome, and will the fluid go away after surgery?,How often should I have follow-up appointments after treatment?

Common questions about Ovarian fibroma

What is Ovarian fibroma?

Ovarian fibroma is a rare, 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. Ovarian fibromas make up a small percentage of all ovarian tumors, and they are most commonly found in women who are middle-aged or older, typically around or after menopause. These tumors are usually solid, slow-growing, and found on one ovary. Most ovarian fibromas do not produce hormones, so they often grow silently without causing obvious symptoms at first. As the tumor gets l

How is Ovarian fibroma inherited?

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

At what age does Ovarian fibroma typically begin?

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

Which specialists treat Ovarian fibroma?

8 specialists and care centers treating Ovarian fibroma are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.