Đặc điểm dịch tễ lâm sàng, cận lâm sàng của trẻ suy giáp bẩm sinh tại Bệnh viện Nhi Trung ương

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Tác giả: Mạnh Hùng Đỗ, Việt Khánh Nguyễn, Anh Vũ

Ngôn ngữ: Vie

Ký hiệu phân loại:

Thông tin xuất bản: Y học cộng đồng 2022

Mô tả vật lý: 113-119

Bộ sưu tập: Metadata

ID: 407702

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Mô tả đặc điểm lâm sàng, cận lâm sàng của trẻ suy giáp bẩm sinh tại Bệnh viện Nhi Trung ương từ 01/2015 - 01/2020
Đối tượng và phương pháp nghiên cứu: Chúng tôi chọn được 52 bệnh nhi được chẩn đoán suy giáp bẩm sinh và điều trị nội trú tại Bệnh viện Nhi Trung ương từ 01/2015 - 01/2020
Phương pháp: Mô tả hồi cứu
Kết quả: Qua nghiên cứu 52 bệnh nhi chúng tôi thu được kết quả như sau: phần lớn trẻ SGBS có thể phát hiện được sớm trước 3 tuổi, thậm chí trong độ tuổi sơ sinh. Dấu hiệu nghi ngờ là táo bón đi kèm với phù nhiêm, vàng da kéo dài, chậm phát triển tâm vận động, TSH>
100 µU/ml, FT3 từ 1-2pg/ml, FT4<
0,4ng/dl, thiếu máu và chậm trưởng thành xương trên X quang
Kết luận: Phần lớn trẻ SGBS có thể phát hiện được sớm trước 3 tuổi
Dấu hiệu nghi ngờ là táo bón đi kèm với phù nhiêm, vàng da kéo dài, chậm phát triển tâm vận động, TSH>
100 µU/ml, FT3 từ 1-2pg/ml, FT4<
0,4ng/dl, thiếu máu và chậm trưởng thành xương trên X quang., Tóm tắt tiếng anh, Describe the clinical and subclinical characteristics of children with congenital hypothyroidism at the National Hospital of Pediatrics from January 2015 to January 2020
Subjects: We selected 52 pediatric patients diagnosed with congenital hypothyroidism and inpatient treatment at the National Hospital of Pediatrics from January 2015 to January 2020
Methods: Describe retrospective
Results: Through the study of 52 pediatric patients, we obtained the following results: most children with congenital hypothyroidism can be detected as early as 3 years, even in infancy. A suspected >
ign of constipation is accompanied by edema, prolonged jaundice, and delayed psychomotor development. Up to 86.5% had THS>
100 micro U / ml, 78.8% had an FT3 of 1-2 pg / ml, 73.1% had an 7T4 <
0.4 ng / dl, 61.5% had anemia, 100% had delayed bone maturation on radiographs
Conclusions: Most children with congenital hypothyroidism can be detected as early as 3 years. A suspected sign of constipation is accompanied by edema, prolonged jaundice, and delayed psychomotor development. TSH >
100 micro U/ml
FT3 of 1-2 pg/ml
FT4 <
0.4 ng/dl
anemia
delayed bone maturation on radiographs.

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