Year 2021,
Volume: 7 Issue: 1, 143 - 146, 30.04.2021
Ece Bahceci
,
Murat Hosgoren
Keziban Doğan
,
Emine Öztürk
References
- 1 Samanta D, Cobb S, Arya K. Sneddon Syndrome: A Comprehensive Overview J Stroke Cerebrovasc Dis.2019; 8:2098-2108
- 2 Zelger B,Sepp N, Stockhammer G, et al. Fritsch PO. Sneddon's Syndrome:A Longterm Follow-up of 21 Patients Arch Dermatol. 1993;129:437-447.
- 3 Sneddon IB. Cerebrovascular lesions and livedo reticularis. Br J Dermatol. 1965;77:180-5.
- 4 Wu S, Xu Z, Liang H. Sneddon’s syndrome: a comprehensive review of the literature Orphanet J Rare Dis. 2014;9:215.
- 5 Tourbah A, Piette JC,Iba-Zizen MT, Lyon-Caen O, Godeau P,Francès C. The Natural Course of Cerebral Lesions in Sneddon Syndrome Arch Neurol 1997;54:53-60.
- 6 Dikova Ch, Kolarov G, Baleva M, Nikolov K. Spontaneous abortions in Sneddon's syndrome Akush Ginekol.2000;39:24-5.
- 7 Baleva M, Boyanovsky B, Nikolov K, Kolarov Z, Nikolova M. High levels of IgA anticardiolipin antibodies in patients with systemic lupus erythematosus, HenochSchoenlein purpura, Sneddon's syndrome and recurrent pregnancy loss. Thromb Haemost.1999;82:1774-5.
- 8 Dietl J, Stroppel G, Poremba M, Lubach D. Sneddon's syndrome and pregnancy; a case report. Eur J Obstet Gynecol Reprod Biol.1991 10;39:219-21
A case with sneddon syndrome combining with preeclampsia and intrahepatic cholestasis of pregnancy
Year 2021,
Volume: 7 Issue: 1, 143 - 146, 30.04.2021
Ece Bahceci
,
Murat Hosgoren
Keziban Doğan
,
Emine Öztürk
Abstract
Sneddon's syndrome (SS) is a rarely seen thrombotic vasculopathy characterized by the combination of ischemic cerebrovascular disease with livedo racemose (LR) and mainly affects young women in the third decade of life. We present a case of an 32 year old women diagnosed with SS 17 years ago, admitted to our emergency department when she was 37 weeks pregnant, and diagnosed as having superimposed severe preeclampsia and intrahepatic cholestasis of pregnancy, who had an emergency cesarean section. There are very few case reports presenting the relationship between pregnancy and SS and a possible relationship between this syndrome and preeclampsia or cholestasis has not yet been shown. We think that our case presentation may become important to contribute literature.
References
- 1 Samanta D, Cobb S, Arya K. Sneddon Syndrome: A Comprehensive Overview J Stroke Cerebrovasc Dis.2019; 8:2098-2108
- 2 Zelger B,Sepp N, Stockhammer G, et al. Fritsch PO. Sneddon's Syndrome:A Longterm Follow-up of 21 Patients Arch Dermatol. 1993;129:437-447.
- 3 Sneddon IB. Cerebrovascular lesions and livedo reticularis. Br J Dermatol. 1965;77:180-5.
- 4 Wu S, Xu Z, Liang H. Sneddon’s syndrome: a comprehensive review of the literature Orphanet J Rare Dis. 2014;9:215.
- 5 Tourbah A, Piette JC,Iba-Zizen MT, Lyon-Caen O, Godeau P,Francès C. The Natural Course of Cerebral Lesions in Sneddon Syndrome Arch Neurol 1997;54:53-60.
- 6 Dikova Ch, Kolarov G, Baleva M, Nikolov K. Spontaneous abortions in Sneddon's syndrome Akush Ginekol.2000;39:24-5.
- 7 Baleva M, Boyanovsky B, Nikolov K, Kolarov Z, Nikolova M. High levels of IgA anticardiolipin antibodies in patients with systemic lupus erythematosus, HenochSchoenlein purpura, Sneddon's syndrome and recurrent pregnancy loss. Thromb Haemost.1999;82:1774-5.
- 8 Dietl J, Stroppel G, Poremba M, Lubach D. Sneddon's syndrome and pregnancy; a case report. Eur J Obstet Gynecol Reprod Biol.1991 10;39:219-21