The association of myasthenia gravis with multiple hamartoma syndrome (Cowden disease)
β Scribed by Tatsuhiko Yuasa; Masaharu Hanano; Fumi Ohshima; Tadao Tsubaki
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 225 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Cowden disease (CD) is a rare, autosomal dominant inherited cancer syndrome characterized by multiple benign and malignant lesions in a wide spectrum of tissues. While individuals with CD have an increased risk of breast and thyroid neoplasms, the primary features of CD are hamartomas. The gene for
and Review of the Literature with Special Reference to Carney Syndrome W e read the article of Kiryu et al. with great interest. 1 They re- ported a case of multiple chondromatous hamartoma of the lung and reviewed the literature. However, the case that we published in 1997 was not included among th
## BACKGROUND. Multiple chondromatous hamartomas of the lung, which are very rare, are a feature of Carney syndrome. The relation between the two entities is not clear.