Altahan Rahaf, Al Mugairi Areej
Division of Hematopathology, Department of Pathology and Laboratory Medicine King Abdul Aziz Medical City Riyadh Saudi Arabia.
Clin Case Rep. 2019 Jul 30;7(9):1809-1810. doi: 10.1002/ccr3.2291. eCollection 2019 Sep.
We present images (Figure 1A-D) of a preterm girl who had severe anemia due to HDFN caused by maternal anti-C and anti-D alloantibodies. These images show erythrophagocytosis, which is a very interesting and rarely encountered feature. We believe that physicians taking care of such patients should be more aware of this characteristic yet under-detected finding.
我们展示了一名早产女婴的图像（图1A - D），她因母亲的抗 - C和抗 - D同种抗体导致的新生儿溶血病而患有严重贫血。这些图像显示了红细胞吞噬现象，这是一个非常有趣且罕见的特征。我们认为，照料此类患者的医生应该更加了解这一特征明显但却未被充分检测到的发现。
