Osteosarcomatosis with rothmund-thomson syndrome

We describe the second reported case of multicentric osteosarcoma associated with Rothmund-Thomson syndrome (RTS), a rare hereditary cancer-prone genodermatosis characterized by typical cutaneous lesions and other non-dermatological pathological manifestations, particularly skeletal changes. A high...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: El-Khoury, J.M. (author)
مؤلفون آخرون: Haddad, S.N. (author), Atallah, N.G. (author)
التنسيق: article
منشور في: 1977
الوصول للمادة أونلاين:http://hdl.handle.net/10725/10478
https://doi.org/10.1259/bjr.70.830.9135453
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://www.birpublications.org/doi/abs/10.1259/bjr.70.830.9135453
الوسوم: إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
_version_ 1864513486629896192
author El-Khoury, J.M.
author2 Haddad, S.N.
Atallah, N.G.
author2_role author
author
author_facet El-Khoury, J.M.
Haddad, S.N.
Atallah, N.G.
author_role author
dc.creator.none.fl_str_mv El-Khoury, J.M.
Haddad, S.N.
Atallah, N.G.
dc.date.none.fl_str_mv 1977
2019-04-17T13:35:46Z
2019-04-17T13:35:46Z
2019-04-17
dc.identifier.none.fl_str_mv 1748-880X
http://hdl.handle.net/10725/10478
https://doi.org/10.1259/bjr.70.830.9135453
El-Khoury, J. M., Haddad, S. N., & Atallah, N. G. (1997). Osteosarcomatosis with Rothmund-Thomson syndrome. The British journal of radiology, 70(830), 215-218.
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://www.birpublications.org/doi/abs/10.1259/bjr.70.830.9135453
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv The British journal of radiology
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.title.none.fl_str_mv Osteosarcomatosis with rothmund-thomson syndrome
dc.type.none.fl_str_mv Article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description We describe the second reported case of multicentric osteosarcoma associated with Rothmund-Thomson syndrome (RTS), a rare hereditary cancer-prone genodermatosis characterized by typical cutaneous lesions and other non-dermatological pathological manifestations, particularly skeletal changes. A high incidence of malignant disorders has been found in RTS patients. This could be explained by the diminished capacity of DNA-repair demonstrated in the fibroblasts of RTS patients following exposure to oncogenic stimuli. The severe cutaneous lesions and the benign bone lesions found in RTS may be considered a predisposing factor to the particularly frequent skin carcinoma and osteogenic sarcoma encountered in these cancer-prone patients. A brief review of the literature is given, with a discussion of the association between these two rare conditions.
eu_rights_str_mv openAccess
format article
id LAURepo_ed05017604523dfd72d53bec041e760c
identifier_str_mv 1748-880X
El-Khoury, J. M., Haddad, S. N., & Atallah, N. G. (1997). Osteosarcomatosis with Rothmund-Thomson syndrome. The British journal of radiology, 70(830), 215-218.
language_invalid_str_mv en
network_acronym_str LAURepo
network_name_str Lebanese American University repository
oai_identifier_str oai:laur.lau.edu.lb:10725/10478
publishDate 1977
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
spelling Osteosarcomatosis with rothmund-thomson syndromeEl-Khoury, J.M.Haddad, S.N.Atallah, N.G.We describe the second reported case of multicentric osteosarcoma associated with Rothmund-Thomson syndrome (RTS), a rare hereditary cancer-prone genodermatosis characterized by typical cutaneous lesions and other non-dermatological pathological manifestations, particularly skeletal changes. A high incidence of malignant disorders has been found in RTS patients. This could be explained by the diminished capacity of DNA-repair demonstrated in the fibroblasts of RTS patients following exposure to oncogenic stimuli. The severe cutaneous lesions and the benign bone lesions found in RTS may be considered a predisposing factor to the particularly frequent skin carcinoma and osteogenic sarcoma encountered in these cancer-prone patients. A brief review of the literature is given, with a discussion of the association between these two rare conditions.PublishedN/A2019-04-17T13:35:46Z2019-04-17T13:35:46Z19772019-04-17Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1748-880Xhttp://hdl.handle.net/10725/10478https://doi.org/10.1259/bjr.70.830.9135453El-Khoury, J. M., Haddad, S. N., & Atallah, N. G. (1997). Osteosarcomatosis with Rothmund-Thomson syndrome. The British journal of radiology, 70(830), 215-218.http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttps://www.birpublications.org/doi/abs/10.1259/bjr.70.830.9135453enThe British journal of radiologyinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/104782021-03-19T10:45:33Z
spellingShingle Osteosarcomatosis with rothmund-thomson syndrome
El-Khoury, J.M.
status_str publishedVersion
title Osteosarcomatosis with rothmund-thomson syndrome
title_full Osteosarcomatosis with rothmund-thomson syndrome
title_fullStr Osteosarcomatosis with rothmund-thomson syndrome
title_full_unstemmed Osteosarcomatosis with rothmund-thomson syndrome
title_short Osteosarcomatosis with rothmund-thomson syndrome
title_sort Osteosarcomatosis with rothmund-thomson syndrome
url http://hdl.handle.net/10725/10478
https://doi.org/10.1259/bjr.70.830.9135453
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://www.birpublications.org/doi/abs/10.1259/bjr.70.830.9135453