AI Article Synopsis

  • A 45-year-old male sibling donor received pegfilgrastim for stem cell collection, which led to the development of fever and submandibular pain a few days later.
  • After imaging revealed wall thickening in the carotid artery and aorta, he was diagnosed with pegfilgrastim-induced aortitis following extensive testing to rule out other conditions.
  • Treatment with prednisolone quickly resolved the symptoms, and after a careful tapering process, he experienced no relapse over the following months, marking this as the first reported case of its kind.

Article Abstract

A 45-year-old man who was a sibling donor for allogeneic peripheral blood stem cell transplantation (allo-PBSCT) was administered 7.2 mg of pegfilgrastim for stem cell collection. Peripheral blood stem cells were collected 4 days after administration of pegfilgrastim (Day 4) and 4.32 × 10 /kg of CD34-positive cells per recipient body weight were obtained. Fever of 38 ℃ or higher and left submandibular pain appeared on Day 6. Ultrasonography and contrast-enhanced computed tomography (CT) showed wall thickening of the carotid artery and the abdominal aorta. We carefully excluded the possibilities of cardiovascular and autoimmune diseases by thorough examination, and ultimately diagnosed pegfilgrastim-induced aortitis. The patient's fever resolved rapidly after treatment with prednisolone (PSL) 1 mg/kg. We began to taper PSL after eight days. Sixty-one days after starting PSL, we confirmed that abdominal aortic wall thickening had improved by contrast-enhanced CT. We continued to taper off PSL and stopped 141 days later with no relapse thereafter. This is the first case report of pegfilgrastim-induced aortitis in an allo-PBSCT donor. Careful monitoring is warranted when administering pegfilgrastim to donors even without past medical history.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673976PMC
http://dx.doi.org/10.1007/s12185-023-03649-0DOI Listing

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