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09 August 2021: Articles

Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages

Rare disease

Shin-ya Katsuragi A , Etsuko Hirose A , Yoshifumi Arai A , Yoshiro Otsuki C* , Shigeru Ohki B , Hiroshi Kobayashi A

DOI: 10.12659/AJCR.932450

Am J Case Rep 2021; 22:e932450

Figure 4. (A) Geographically fused infarct is found in the spleen. (B) The splenic infarction (hematoxylin and eosin staining [H&E], ×40, inset: organized thrombus). (C) Renal cortex (H&E, ×100, inset: immature glomeruli).

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923