Pathan Sajidkhan
JIIU's Indian Institute of Medical Science and Research, Warudi, Badnapur, Maharashtra India.
Sadeqa ENT Hospital, Near Head Post Office, Juna Bazaar, Aurangabad, Maharashtra 431001 India.
Indian J Otolaryngol Head Neck Surg. 2025 Jan;77(1):553-555. doi: 10.1007/s12070-024-05192-8. Epub 2024 Nov 11.
In this case we report rare clinical entity of Millers syndrome in a small child of 6 years. It is basically an autosomal recessive condition characterized by anomalies of face and limbs such as malar hypoplasia, micrognathia, cleft lip and palate, restricted airway, bones and joints malformations [1, 2]. In this child apart from all these features we came across bleeding nasal masses attached to the inferior tubinates, which were causing complete nasal obstruction. Nasal mass was surgically removed and sent for histopathological examination. It turned out to be nasal polyp with very high vascularity containing mucopolysaccharide material.
在此病例中,我们报告了一名6岁幼儿患罕见的米勒综合征临床病例。这基本上是一种常染色体隐性疾病,其特征为面部和四肢异常,如颧骨发育不全、小颌畸形、唇腭裂、气道受限、骨骼和关节畸形[1,2]。在这名患儿中,除了所有这些特征外,我们还发现附着在下鼻甲上的出血性鼻肿物,导致完全性鼻阻塞。鼻肿物经手术切除并送去做组织病理学检查。结果显示为血管非常丰富且含有黏多糖物质的鼻息肉。