点状根状软骨发育不良的细胞学表现:一种罕见的骨骼发育不良

P. Agarwal, Ashok Kumar, Ashutosh Kumar Singh, Shipra Singh, A. Parihar
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摘要

点状软骨发育不良(CDP)是一种罕见的骨骼发育不良,其特征是关节周围和软骨内的点状、点状钙化。一个4个月大的女婴因踝关节肿胀和发育不全而被临床怀疑为肉瘤而就诊于我们。细针抽吸(FNA)涂片无细胞,仅有钙化沉积。注意鼻部凹陷与额部隆起的临床相关性。我们怀疑这是一例先天性骨骼发育不良。对病变进行x线平片检查,发现踝关节骨处有点状钙化,符合点状软骨发育不良。本病例是描述点状软骨发育不良细胞学的一个指标病例。CDP主要是一种影像学诊断的病变,但通过本病例了解其细胞学图像将使病理学家在遇到此类病例时都能意识到。管理基本上是支持性和康复性的。
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Cytological findings of rhizomelic chondrodysplasia punctata: A rare skeletal dysplasia
Chondrodysplasia punctata (CDP) is a rare, skeletal dysplasia characterized by stippled, punctuate calcifications around joints and within cartilages. A 4 months old female infant presented to us for aspiration cytology with clinical suspicion of sarcoma due to complaint of ankle swelling and failure to thrive. Fine needle aspiration (FNA) smears were acellular with only calcific deposits. On clinical co-relation depressed nose and frontal bossing were noted. We suspected it to be a case of congenital skeletal dysplasia. Plain X-ray of the lesion was ordered and it revealed stippled calcification in place of ankle bones consistent with chondrodysplasia punctata. The present case is an index case describing the cytology of chondrodysplasia punctata. CDP is mainly a radiologically diagnosed lesion, however the knowledge of its cytological picture through this case will make pathologists alike aware if they encounter such case. The management is basically supportive and rehabilitative.
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