ABSTRACT NUMBER: ESOC2026A1355 SEVERE POST-THROMBOLYSIS HYPOFIBRINOGENEMIA REVEALING CONGENITAL FACTOR VII DEFICIENCY: A CASE REPORT
Mariarosaria Medici, Laura Vandelli, Maria Luisa Dell'acqua, Laura Giacobazzi, Gabriele Vandelli, Livio Picchetto, Francesca Rosafio, Manuel Menabue, Guido Bigliardi · 2026
Read ABSTRACT NUMBER: ESOC2026A1355 SEVERE POST-THROMBOLYSIS HYPOFIBRINOGENEMIA REVEALING CONGENITAL FACTOR VII DEFICIENCY: A CASE REPORT by Mariarosaria Medici, Laura Vandelli, Maria Luisa Dell'acqua, Laura Giacobazzi, Gabriele Vandelli, Livio Picchetto, Francesca Rosafio, Manuel Menabue, Guido Bigliardi (2026) in the Tower of Babel, a free online library of public-domain works preserved in clean, searchable text. No sign-up. The full text is served as a plain-text file at a predictable URL, where text is present: https://antarctic-labs.com/tower-of-babel/pmc-13144854.txt.
Description
Mariarosaria Medici and co-authors report a stroke case where clot-busting care masked a rare blood flaw, in an abstract from 2026. A 62-year-old woman came in with weak, clumsy movement on her right side. With no bar to care, she got the standard vein drug that breaks clots.
Two hours on, her fibrinogen, a key clot part, read as zero, and her blood would not clot in the lab tool. Doses of fibrinogen lifted it just a touch. More checks found the root: she was born with a mid-level lack of factor VII, a clot helper, a flaw that had sat mute for years. She healed in full with no bleeds. A heart drug was then started with care. The team urges close blood watch after such care.
Catalog record
| CREATOR | Mariarosaria Medici, Laura Vandelli, Maria Luisa Dell'acqua, Laura Giacobazzi, Gabriele Vandelli, Livio Picchetto, Francesca Rosafio, Manuel Menabue, Guido Bigliardi |
|---|---|
| YEAR | 2026 |
| COLLECTION | PAPERS |
| FORMAT | TXT |
| FILE SIZE | 2 KB |
| VERSION | 1.0 |
| LICENSE | CC BY 4.0 |
| RIGHTS | CC BY |
| SOURCE | Europe PMC |