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Case Reports
. 2022 Oct 22;22(1):391.
doi: 10.1186/s12883-022-02918-5.

Multiple cerebral infarctions due to calcified amorphous tumor growing rapidly from an antecedent infection and decreasing rapidly by detachment of fibrin and antithrombotic drugs: a case report

Affiliations
Case Reports

Multiple cerebral infarctions due to calcified amorphous tumor growing rapidly from an antecedent infection and decreasing rapidly by detachment of fibrin and antithrombotic drugs: a case report

Motoya Kimura et al. BMC Neurol. .

Abstract

Background: Calcified amorphous tumor (CAT) of the heart is a rare non-neoplastic intracardiac mass, a calcium deposition surrounded by amorphous fibrous tissue, and possibly causes cerebral embolism. Even rarer is CAT associated with infection, and no CAT with antecedent infection has been reported to our knowledge. In addition, although some CAT in patients on hemodialysis has been reported to grow rapidly, no case has been reported on CAT that grew and diminished rapidly in a short period of time. Here, we report the case of an 82-year-old Japanese woman with normal renal function who developed multiple cerebral infarctions due to CAT that grew rapidly, associated with inflammation from an antecedent infection, and diminished rapidly by detachment of fibrin on the mass surface and antithrombotic drugs.

Case presentation: The patient developed fever after dental treatment and found musical hallucination on the left ear worsened in degree and frequency. In a nearby clinic, she was treated with antibiotics, and her body temperature turned to normal in approximately 1 month. She presented to our hospital for workup on the worsened musical hallucination. Magnetic resonance imaging (MRI) showed multiple cerebral infarctions, and transthoracic echocardiography (TTE) revealed an immobile hyperechoic mass with an acoustic shadow arising from a posterior cusp of the mitral valve. CAT was suspected and treated with apixaban and aspirin. Follow-up MRI and TTE showed newly developed multiple cerebral infarctions and rapidly diminished CAT. Cardiac surgery was performed to resect the CAT. The pathological findings showed calcifications surrounded by amorphous fibrous tissue including fibrin, indicating CAT. The patient's symptoms improved and no cerebral infarctions recurred in 4 months follow-up.

Conclusion: Inflammation from an antecedent infection can cause CAT to grow rapidly. Fibrous tissue including fibrin may attach to the surface of CAT, resulting in multiple cerebral infarctions. Fibrous tissue may detach and disappear by antithrombotic drugs, leading to a rapid diminishment of CAT in size.

Keywords: Antecedent infection; Calcified amorphous tumor; Case report; Fibrin; Multiple cerebral infarctions.

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Conflict of interest statement

The authors declare that they have no known conflict of interest or personal relationships that could have appeared to influence the work reported in this paper.

Figures

Fig. 1
Fig. 1
Serial transthoracic echocardiographs. A hyperechoic lesion or an acoustic shadow were not observed 7 months before the admission (A). An immobile hyperechoic 14.9 × 12.1 mm mass with an acoustic shadow arising from a posterior cusp of the mitral valve on admission (B, arrowheads). The mass was decreased to 13.8 × 9.7 mm in size on the 9 th day of admission (C, arrowheads)
Fig. 2
Fig. 2
Brain magnetic resonance images on diffusion-weighted imaging on admission. Multiple small lesions, which showed high intensity on diffusion-weighted imaging, are seen on the right cerebellum, left thalamus and frontal lobe, bilateral parietal lobe, occipital lobe, and nucleus basalis (A-F). Magnetic resonance angiography was unremarkable (G and H)
Fig. 3
Fig. 3
Pathological images of the resected tissue. Amorphous fibrous tissue surrounding the multiple nodular calcifications, lymphocyte infiltration and hemosiderin deposition were confirmed in the fibrous tissue (A, arrowheads). Neoangiogenesis occured in the mitral valve (B, arrowheads). CAT was stained by phosphotungstic acid-hematoxylin (PTAH) stain (C) and Von Kossa stain (D). Fibrin around CAT and calcification of CAT were shown in blue/purple by PTAH stain (C). Calcification of CAT was shown in black/brown by Von Kossa stain (D). In comparing (C) with (D), the area that was stained in (C) but not in (D) indicated fibrin attached to CAT (C, arrowhead)

References

    1. Reynolds C, Tazelaar HD, Edwards WD. Calcified amorphous tumor of the heart (cardiac CAT) Hum Pathol. 1997;28:601–606. doi: 10.1016/s0046-8177(97)90083-6. - DOI - PubMed
    1. de Hemptinne Q, de Cannière DD, Vandenbossche JL, Unger P. Cardiac calcified amorphous tumor: a systematic review of the literature. Int J Cardiol Heart Vasc. 2015;7:1–5. doi: 10.1016/j.ijcha.2015.01.012. - DOI - PMC - PubMed
    1. Nishiguchi Y, Matsuyama H, Shindo A, Matsuura K, Niwa A, Hirota Y, et al. Cerebral embolism associated with calcified amorphous tumor: a review of cerebral infarction cases. Intern Med. 2021;60:2315–2319. doi: 10.2169/internalmedicine.6262-20. - DOI - PMC - PubMed
    1. Okazaki A, Oyama Y, Hosokawa N, Ban H, Miyaji Y, Moody S. The first report of calcified amorphous tumor associated with infective endocarditis: a case report and review of literature. Am J Case Rep. 2020;21:e922960. doi: 10.12659/AJCR.922960. - DOI - PMC - PubMed
    1. Handa K, Fukui S, Shirakawa Y, Sakamoto T, Kitahara M, Kakizawa Y, et al. Infective calcified amorphous tumor on mitral valve and critical course of left ventricular rupture. J Cardiol Cases. 2021;24:182–185. doi: 10.1016/j.jccase.2021.04.008. - DOI - PMC - PubMed

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