TY - JOUR
T1 - Fatal bilateral pneumothoraces complicating dyskeratosis congenita
T2 - A case report
AU - Boueiz, Adel
AU - Abougergi, Marwan S.
AU - Noujeim, Carlos
AU - Assaf, Edmond Bou
AU - Jamaleddine, Ghassan
PY - 2009
Y1 - 2009
N2 - Introduction. Dyskeratosis congenita is a rare genodermatosis, characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membranes. It is also associated with a variety of non-cutaneous abnormalities such as bone marrow failure, malignancy and pulmonary complications. Among its wide range of clinical manifestations, fatal pneumothorax has rarely been reported. Case presentation. We report the case of a 31-year-old Lebanese woman with dyskeratosis congenita who succumbed to devastating bilateral pneumothoraces. Conclusion. Careful surveillance of patients with dyskeratosis congenita is required as incipient respiratory failure due to pneumothorax may be successfully treated if detected at an early stage.
AB - Introduction. Dyskeratosis congenita is a rare genodermatosis, characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membranes. It is also associated with a variety of non-cutaneous abnormalities such as bone marrow failure, malignancy and pulmonary complications. Among its wide range of clinical manifestations, fatal pneumothorax has rarely been reported. Case presentation. We report the case of a 31-year-old Lebanese woman with dyskeratosis congenita who succumbed to devastating bilateral pneumothoraces. Conclusion. Careful surveillance of patients with dyskeratosis congenita is required as incipient respiratory failure due to pneumothorax may be successfully treated if detected at an early stage.
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U2 - 10.1186/1752-1947-3-6622
DO - 10.1186/1752-1947-3-6622
M3 - Article
C2 - 19830116
AN - SCOPUS:72249096269
SN - 1752-1947
VL - 3
JO - Journal of Medical Case Reports
JF - Journal of Medical Case Reports
M1 - 6622
ER -