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Page Updated: September 03, 2021

Benign Mesothelioma

Pinar Kanlikilicer Page Medically Reviewed and Edited by Pinar Kanlikilicer, PhD

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Fact Checked

This page has been fact checked by a PhD who specializes in cancer research. Sources of information are listed at the bottom of the article.

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We make every attempt to keep our information accurate and up-to-date.

Please Contact Us with any questions or comments.

Benign mesothelioma is a rare but treatable non-malignant form of mesothelioma. Benign tumors may grow in size but do not spread, or metastasize, to other tissues and organs. Treatment is straightforward, usually involving surgery to remove the tumor, and the prognosis is excellent.

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Malignant vs. Benign Mesothelioma

The main difference between these types of tumors is that malignant mesothelioma can spread to other tissues. In contrast, a benign tumor does not spread.

Mesothelioma is rare as a type of cancer, but benign tumors of the mesothelium are even rarer; also, malignant mesothelioma is strongly connected to asbestos exposure, while the benign form has unknown causes.[1]

There are several subtypes of each kind of mesothelioma. Benign tumors can come in different forms, including benign pleura tumors, benign multicystic peritoneal mesothelioma, and papillary mesothelioma.

Of these, benign tumors in the pleura are most common. The peritoneal form is rare, with only about 150 cases ever reported, and papillary mesothelioma is even rarer.[2][3]

Benign Fibrous Pleural Mesothelioma

The most common of these rare benign mesotheliomas forms in the pleura, or the lining of the lungs. In 2004, approximately 500 cases of benign mesothelioma in the pleura were reported.

Most of these tumors first grow in the visceral layer of the pleura, the inner layer surrounding the lungs. Benign pleural tumors can range from small to large, are typically smooth, have fluid-filled cysts, and are often partially calcified. Tumor cells may be fibrous, cellular, mixed, or a combination of fibrous and cellular.

Benign Multicystic Peritoneal Mesothelioma

Even less common is the type of benign mesothelioma that originates in the peritoneum, the epithelium that lines abdominal organs. This type is most common in women of reproductive age, although it can occur in both sexes and at any age.

Benign peritoneal mesothelioma is usually multicystic, meaning they contain multiple, fluid-filled cysts. Based on the reported cases, the prognosis of benign peritoneal mesothelioma is very good.[4]

Well-Differentiated Papillary Mesothelioma

Very few cases of well-differentiated papillary mesothelioma (WDPM) exist. They are mostly benign tumors, although some also have malignant cells.

They are more common in women between thirty and forty and are most likely to arise in the peritoneum. In a few cases, these tumors have developed in the pericardium, the lining around the heart.

Papillary mesothelioma tumors are characterized by papillary structures, which can only be seen under the microscope. The optimal treatment for WDPMP is not clear due to rare incidence rates. Long-term follow-ups are needed to characterize this type of cancer.[3]

Adenomatoid Tumors

Adenomatoid tumors are often seen in the testis or uterus. These tumors are often classified as benign mesotheliomas because they originate in the mesothelium that surrounds the glands.

This type of tumor can become malignant; however, they are most often benign and can be found in the pleura or peritoneum and the testis and uterus.[5]

Complications

Although benign tumors are noncancerous and do not spread to other tissues, they can create problems as they increase in size.

Benign pleural tumors, for instance, can cause some of the same symptoms as malignant pleural mesothelioma. These symptoms include:[1]

  • Tightness in the chest
  • Shortness of breath
  • Chest pains
  • Pleural effusion

If the tumor is a significant size, it can ultimately cause more serious complications, including seizures and coma.

Benign mesothelial tumors of the peritoneum or pericardium may cause similar complications. Complications usually occur when the tumor has grown large enough to cause fluid buildup, resulting in pain or discomfort.

In many cases of peritoneal or pericardial benign tumors, there are no symptoms. The tumor may be found coincidentally if the patient is being screened for something else.

Diagnosis

Diagnosis for benign mesotheliomas may be accidental if no symptoms are apparent; however, the tumor grows large enough to cause discomfort in some cases.

Diagnosis begins with a physical exam and continues with imaging scans. These scans may indicate an unusual mass or lesion, which is expected to be a tumor.[1]

The next step is to determine whether a mass is a benign or malignant tumor, whether it is mesothelioma, and what cell types are involved.

A pathologist can examine the biopsied tumor sample under a microscope to determine if the cells are benign. They can also determine if the biopsied tissue is of a papillary or adenomatoid type.

This histological approach is not always accurate, but immunohistochemical staining can improve that accuracy. This technique uses antibodies to target specific antigens in tumor cells. It can rule out or find cancerous cells with good accuracy.

Treatment

If there are no symptoms and a benign mesothelial tumor is small, it may not require treatment. If the tumor is increasing in size and causing discomfort, the typical treatment is surgery to remove the mass.[1]

Treatments are straightforward surgeries with modest recovery periods. In some cases of benign pleural mesothelioma, a lung segment or an entire lobe may need to be removed. This will require more recovery time and increases the possibility of complications.

Prognosis

The prognosis for benign mesotheliomas is overwhelmingly positive, but, as with surgery, there are risks; however, surgical removal of one of these tumors is completely curative. Some patients may experience a recurrence, but recurrence is typically benign and occurs years later. Survival rates of benign mesothelioma are near 100%.[1]

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Page Medically Reviewed and Edited by Pinar Kanlikilicer, PhD

Pinar Kanlikilicer

Dr. Pinar Kanlikilicer has a PhD in Biomedical Engineering. She completed her 5-years of postdoctoral training in the Department of Experimental Therapeutics at MD Anderson Cancer Center. She is currently working in the field of cancer as a research scientist.

Learn more about Cancer Research Specialist Pinar Kanlikilicer, PhD
References
  1. MedlinePlus. (2018, July 28). Solitary Fibrous Tumor.
    Retrieved from: https://medlineplus.gov/ency/article/000116.htm
  2. Tuncer, A.A., Narci, A., Dilek, F.H., Embleton, D.B., and Cetinkursun, S. (2016, March). Benign Cystic Mesothelioma in a Child: Case Report and Review of the Literature. Balkan Med. J. 33(2), 232-4.
    Retrieved from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924971/
  3. Malpica, A., Sant’Ambrogio, S., Deavers, M.T., and Silva, E.G. (2012, January). Well-Differentiated Papillary Mesothelioma of the Female Peritoneum: A Clinicopathologic Study of 26 Cases. Am. J. Surg. Pathol. 36(1), 117-27.
    Retrieved from: http://www.ncbi.nlm.nih.gov/pubmed/22024662
  4. Want, T.B., Dai, W.G., Liu, D.W., Shi, H.P., and Dong, W.G. (2013, October 21). Diagnosis and Treatment of Benign Multicystic Peritoneal Mesothelioma. World J. Gastroenterol. 19(39), 6689-92.
    Retrieved from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3801387/
  5. Amin, W. and Parwani, A.V. (2009, September). Adenomatoid Tumor of Testis. Clin. Med. Pathol. 2, 17-22.
    Retrieved from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990235/
View All References

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