Pleuropulmonary Blastoma (PPB)
KidsRStrong2 was founded in honor of Isaiah Gamble, who at the young age of 3 was diagnosed with an extremely rare form of lung cancer. In his honor one of our goals and missions is to spread awareness of PPB, as well as various types of pediatric cancer.
The information below is being shared as is directly from the National Organization of Rare Disorders (NORD) website at
NORD gratefully acknowledges Kris Ann Schultz, MD, and Gretchen Williams, BS, CCRP, Cancer and Blood Disorders Program of Children's Hospitals and Clinics of Minnesota, and the International Pleuropulmonary Blastoma Registry, for assistance in the preparation of this report.
Synonyms of Pleuropulmonary Blastoma
cystic mesenchymal hamartoma
mesenchymal cystic hamartoma
pediatric pulmonary blastoma
rhabdomyosarcoma in lung cyst
CPAM/CCAM Type 4
Subdivisions of Pleuropulmonary Blastoma
Type I PPB
Type II PPB
Type III PPB
Pleuropulmonary blastoma (PPB) is a rare childhood cancer occurring in the chest, specifically in the lungs or in the coverings of the lungs called "pleura". Three subtypes of PPB exist and are called Type I, Type II, and Type III PPB. Type I PPB takes the form of one or more cysts in the lungs (air-filled pockets) and may be found in very young children with PPB (from birth to about 2 years of age). Type III PPB is entirely solid tumor. Type II PPB includes both cystic and solid parts. Types II and III PPB tend to be found more often after 2 years of age. Type Ir (the “r” stands for regressed/ regressing) is another type of PPB. Under the microscope Type Ir is similar to Type I PPB, but it does not have cancerous cells. Type I, II, and III PPB are usually found in children under the age of approximately 7-8 years; PPB occurs rarely in older children or teenagers, and even more rarely in adults, but Type Ir PPB may be found at any age. Children with Type I have a better outlook ("prognosis") than children with Types II and III PPB; most Type I PPB patients are cured (89%) but Type I PPB can sometimes recur (“come back”) as Type II or III PPB. Treatment for Type I consists of surgery and possibly chemotherapy. Treatment for Types II and III PPB consists of surgery and chemotherapy and possibly radiation therapy. At present, about 50-70% of children with Types II and III PPB are cured.
PPB is a childhood cancer in the family of cancers called soft tissue cancers, which are scientifically called sarcomas. PPB is, therefore, a soft tissue sarcoma. Physicians classify diseases this way in order to compare features and to compare treatments. PPB occurs in the lungs and is the most common lung cancer of childhood but PPB has no connection to lung cancers in adults that are often related to tobacco use or asbestos exposure. Like many cancers, PPB can spread through the blood to other areas of the body. When a cancer spreads to another part of the body it is called a "metastasis" of the cancer. Types II and III PPB can metastasize. The most common location for a PPB metastasis is the brain. PPB may also spread to remaining part of the lung, bones, liver and rarely to other organs. PPB can also spread by growing directly into tissues next to the lung like the diaphragm.
Signs & Symptoms
Two different sets of symptoms are found in children with PPB, based generally on the child’s age and the type of PPB:
Respiratory Distress Symptoms:
These symptoms tend to be found in Type I PPB in infants and toddlers (under age 2 years). Respiratory distress or breathing difficulty (dyspnea) may be mild to severe. Large pockets of air in the chest may prevent normal breathing. The air may be in large pockets of air in the lung (cysts) that compress the normal lung. Air also sometimes escapes from cysts into the chest cavity (pneumothorax). A chest x-ray will discover these air pockets and further investigations will lead to surgery to remove them.
Pneumonia/General Illness Symptoms:
These symptoms tend to be found in children with Types II and III PPB. These children are usually older than 2 years of age. These are mostly solid-tumor or partly solid-partly cystic PPBs. Symptoms of a general illness which may appear to be pneumonia are cough, fever, difficulty breathing, fatigue, loss of energy and decreased appetite. Chest or abdominal pain may also occur. Occasionally there is weight loss. A chest x-ray will show a problem that may look like pneumonia (lung infection). Because PPB is rare and other condition of the lung are more common, PPB may not be suspected when a child has these symptoms. Children are often treated with antibiotics for 2-3 weeks, but they do not get better. Further investigations are done, such as a chest CT scan; these tests raise the possibility of a tumor in the chest/lung and surgery is done.
Sometimes PPB occurs without any other conditions in the individual or family but PPB may also be an indication of an underlying mutation in a DICER1 gene (see Related Disorders).
PPB occurs in boys and girls approximately equally. Children under the age of 7-8 years are most often affected, but rarely teenagers or young adults may be diagnosed with PPB. Other conditions sometimes associated with PPB may be seen in individuals throughout the life span (see Related Disorders).
In about 40% of children with PPB there are other childhood cancers or abnormalities in the PPB patient or in their immediate or extended family. This is known as the PPB familial cancer syndrome or DICER1 syndrome. Genetic research has led to the discovery that the DICER1 gene is often mutated in individuals with PPB and in individuals with a variety of other conditions. These other conditions include lung cysts, kidney cysts or tumors, ovarian tumors in children or adults, thyroid nodules or tumors (sometimes malignant), and various other cancers and non-malignant (non cancerous) diseases. All of these are in the DICER1 related spectrum of diseases and conditions. It should be emphasized that many children and adults in these families have no medical problems.
When a DICER gene mutation is found, specific screening studies may be recommended to look for PPB and other conditions known to be related to DICER1. Chest screening (by chest x-ray or chest CT) for young children known to have the DICER1 gene mutation but no symptoms has in some cases allowed PPB to be diagnosed when it’s at the earliest and most curable stage.
When a child presents with symptoms of PPB, a chest x-ray may show an air filled pocket (cyst) or a solid mass. Chest CT may be performed to look at the lungs in more detail. Surgery, either a biopsy or removal of the cyst or mass, is performed to diagnose and often remove the tumor. Microscopic examination of the specimen is needed. Consultation with the International PPB Registry pathology specialists is often helpful in confirming the diagnosis.
After surgery to remove Type I PPB, some physicians recommend use of chemotherapy to attempt to remove any remaining small collections of malignant cells; some physicians recommend watchful waiting. Radiation therapy is not used for Type I PPB. If Type I PPB recurs in a child as Type II or Type III PPB, then the treatments for Types II and III disease must be used.
Type II and III PPB are both serious (aggressive) malignancies. Surgery is the first step in treatment but sometimes due to the size and location of the tumor, only biopsy can be performed. This would be followed by chemotherapy to attempt to shrink the remaining tumor and remove the malignant cells left behind after surgery. Sometimes radiation therapy is also used.
The chemotherapy drugs usually used for treatment of PPB are the same or similar to drugs used for more common childhood cancers. Even though PPB is rare, pediatric cancer specialists have experience using these drugs. Their use in PPB patients is guided by their use in other children.
The use of radiation therapy is highly individualized in PPB patients. In general if there is a small area of tumor which could not be removed by surgery and which does not seem to disappear with chemotherapy, then radiation may be considered. Radiation can damage lung tissue so the doses and locations of radiation therapy are limited by the radiation oncology team. When PPB spreads to the brain, surgery followed by radiation therapy is often advised.
When the kinds of standard treatments outlined above are not successful at eliminating PPB, other therapies are often tried. Chemotherapy drugs for which there is not as much experience in PPB may be recommended. Sometimes new chemotherapy drugs are tried experimentally. Families will always be told the nature of the drugs which are being recommended for use in their child.
Another possible therapy for PPB is high dose chemotherapy followed by autologous stem cell transplantation. This overall approach may be useful in cases where PPB has not been eliminated by more standard therapy.
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government website.
For information about clinical trials being conducted at the National Institutes of Health (NIH) Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Toll free: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
For information about clinical trials conducted in Europe, contact:
Research into the inheritance patterns in PPB patients and their families has already led to the understanding that the DICER1 gene mutation is the reason why some families have a tendency to develop PPB or other problems. Specific screening for PPB and other conditions known to be related to PPB may be requested for anyone who has the DICER1 gene mutation. This research is ongoing. Please contact the International PPB Registry for more information about this study:
The International Pleuropulmonary Blastoma Registry
Phone: 612-813-7115 Gretchen Williams, BS, CCRP or Kris Ann Schultz, MD
Children’s Hospital and Clinics of Minnesota
2545 Chicago Ave. S.
Minneapolis, MN 55404
PO Box 8126
Gaithersburg, MD 20898-8126
Phone: (301) 251-4925
Toll-free: (888) 205-2311
1649 North Pacana Way
Green Valley, AZ 85614 USA
SELECT JOURNAL ARTICLES
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