| Literature DB >> 36149532 |
Shiori Kinoshita1, Hirokazu Komatsu2, Haruna Fujinami1, Takashi Yoshida1, Tomotaka Suzuki1, Tomoko Narita1, Asahi Ito1, Masaki Ri1, Shigeru Kusumoto1, Shinsuke Iida1.
Abstract
We report a case of recurrent pain attacks during romiplostim treatment in a woman with immune thrombocytopenia carrying a heterozygous MEFV mutation. Five months after starting treatment with romiplostim for immune thrombocytopenia, she was diagnosed with idiopathic pericarditis. She was switched to eltrombopag, but thrombocytopenia did not improve. Romiplostim was restarted 7 months later, although she then developed recurrent right hypochondrial pain. The pain typically occurred three days after the romiplostim injection and resolved two days later. She had never experienced such recurrent pain before starting romiplostim or after discontinuing it. Genetic analysis showed that she carried a heterozygous R202Q alteration in exon 2 of the MEFV gene. MEFV mutation is known to cause familial Mediterranean fever, which is characterized by symptoms such as recurrent fever, abdominal and chest pain, arthritis, and pericarditis. This case suggests that romiplostim has the potential to trigger recurrent pain/inflammation attacks in individuals with systemic inflammatory abnormalities.Entities:
Keywords: Familial Mediterranean Fever; Immune thrombocytopenia; MEFV; Romiplostim
Year: 2022 PMID: 36149532 DOI: 10.1007/s12185-022-03453-2
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.319