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The International Pleuropulmonary Blastoma Registry
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Critical Issues


Constitutional & Familial Issues: Genetics of PPB:


A Very Rare Disease: Enrolling Patients in the Registry


Cerebral Metastases in PPB - Surveillance Recommended


Genetic Study of PPB


PPB Associated with Cystic Nephroma and Other Renal Tumors


Type I PPB: Treatment Issues


Type II and III THERAPY RECOMMENDATION CHANGE

Join Our PPB Study

Whats New

04/02/2008
2008 PPB FAMILY WEEKEND--The brochures were mailed today!

02/15/2007
THERAPY CHANGE: PPB Types II and III

11/15/2006
PPB, Cystic Nephroma & Small Bowel Polyps

10/01/2005
Genetic Study in PPB - PPB Tissue Bank

Background and Purpose
This website provides information For Families and For Physicians/Caregivers on the rare childhood chest tumor known as “pleuropulmonary blastoma” or “PPB”. This tumor has occurred for years, but because of its rarity, it has come under concerted medical scrutiny only since the mid-1980’s. With the cooperation of families and physicians all over the world, we have been collecting cases of PPB for 20 years. Through this accumulation of information, we have begun to understand some of the biological and treatment issues of this disease and have published several articles (see Registry Publications). Of course, many others have also made important observations and published information (see Bibliography). We continue to collect cases and we ask for help in this regard from all families and all caregivers .

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Data and recommendations on this site are conscientiously presented but some are unpublished observations and have not undergone peer review. Consultation with the Registry is encouraged to clarify any topics. The International PPB Registry advises caution in the citation of website information.