Literature DB >> 22468940

Follicular thyroid carcinoma arising after hematopoietic stem cell transplantation in a child with pleuropulmonary blastoma.

Seung Han Shin1, Jong Hyung Yoon, Meong Hi Son, Su-Jin Kim, Seog-Yun Park, Hyun Young Kim, Hyun-Sung Lee, Hyeon Jin Park, Byung-Kiu Park.   

Abstract

BACKGROUND: Pleuropulmonary blastoma (PPB) is a rare and aggressive intrathoracic neoplasm that is associated with other dysplastic or neoplastic conditions. The prognosis, especially of type II (cystic and solid) and type III (solid) PPB, is poor. High-dose chemotherapy (HDC) and hematopoietic stem cell transplantation (HSCT) have been attempted to improve survival rates. We report the development of follicular thyroid carcinoma in a girl who was treated at a young age for PPB.
SUMMARY: A 23-month-old girl was evaluated for a clinical diagnosis of pneumonia and was found to have a mass in the left lung that grew rapidly. It was removed and diagnosed as a PPB. At the age of two, she was referred to our hospital for further treatment. She received adjuvant chemotherapy for 6 months but developed a recurred mass in her back at 4.3 years of age. After removal of the mass, she was given a salvage chemotherapy followed by HDC and HSCT but not radiation treatment between 4.4 and 4.9 years of age. At the age of seven, after 2 years without treatment, she presented with multiple thyroid nodules in both lobes that steadily grew over the next 2 years. At the age of nine, she underwent total thyroidectomy, which revealed an invasive follicular carcinoma. She remained without clinical evidence of thyroid cancer for one year since the surgery. Radiation therapy was not administered because of the concerns of causing another malignancy. A literature search combined with the present case indicated that, of the five living patients who had been treated with HDC and HSCT, three developed a follicular thyroid carcinoma.
CONCLUSIONS: The high prevalence (3/5, 60%) of follicular thyroid carcinoma in patients with PPB who were treated with HDC and HSCT is striking. This suggests that, in patients with PPB, either HDC or HSCT contributes to the development of thyroid cancer. Clinicians should be advised of the high risk of thyroid carcinoma occurrence when HDC and HSCT are being contemplated in children with PPB.

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Year:  2012        PMID: 22468940     DOI: 10.1089/thy.2011.0161

Source DB:  PubMed          Journal:  Thyroid        ISSN: 1050-7256            Impact factor:   6.568


  5 in total

Review 1.  Proceedings of the North American Society of Head and Neck Pathology, Los Angeles, CA, March 20, 2022: DICER1-Related Thyroid Tumors.

Authors:  Madeline Sauer; Justine A Barletta
Journal:  Head Neck Pathol       Date:  2022-03-21

Review 2.  Imaging of DICER1 syndrome.

Authors:  R Paul Guillerman; William D Foulkes; John R Priest
Journal:  Pediatr Radiol       Date:  2019-10-16

3.  Quantification of Thyroid Cancer and Multinodular Goiter Risk in the DICER1 Syndrome: A Family-Based Cohort Study.

Authors:  Nicholas E Khan; Andrew J Bauer; Kris Ann P Schultz; Leslie Doros; Rosamma M Decastro; Alexander Ling; Maya B Lodish; Laura A Harney; Ron G Kase; Ann G Carr; Christopher T Rossi; Amanda Field; Anne K Harris; Gretchen M Williams; Louis P Dehner; Yoav H Messinger; D Ashley Hill; Douglas R Stewart
Journal:  J Clin Endocrinol Metab       Date:  2017-05-01       Impact factor: 5.958

Review 4.  DICER1 tumor predisposition syndrome: an evolving story initiated with the pleuropulmonary blastoma.

Authors:  Iván A González; Douglas R Stewart; Kris Ann P Schultz; Amanda P Field; D Ashley Hill; Louis P Dehner
Journal:  Mod Pathol       Date:  2021-10-01       Impact factor: 7.842

5.  Distinct DICER1 Hotspot Mutations Identify Bilateral Tumors as Separate Events.

Authors:  Kenneth S Chen; Sarai H Stuart; Emily K Stroup; Abhay S Shukla; Jason Wang; Veena Rajaram; Gordan M Vujanic; Tamra Slone; Dinesh Rakheja; James F Amatruda
Journal:  JCO Precis Oncol       Date:  2018-04-25
  5 in total

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