Sinkar Prachi, Arakeri Surekha Ulhas
Postgraduate Student, Department of Pathology, BLDE University's Shri BM Patil Medical College, Hospital and Research Centre, Vijayapur, Karnataka, India.
Professor, Department of Pathology, BLDE University's Shri BM Patil Medical College, Hospital and Research Centre, Vijayapur, Karnataka, India.
J Clin Diagn Res. 2017 Mar;11(3):EC28-EC31. doi: 10.7860/JCDR/2017/20882.9532. Epub 2017 Mar 1.
Need for minimal turnaround time for assessing Fine Needle Aspiration Cytology (FNAC) has encouraged innovations in staining techniques that require lesser staining time with unequivocal cell morphology. The standard protocol for conventional Papanicolaou (PAP) stain requires about 40 minutes. To overcome this, Ultrafast Papanicolaou (UFP) stain was introduced which reduces staining time to 90 seconds and also enhances the quality. However, reagents required for this were not easily available hence, Modified Ultrafast Papanicolaou (MUFP) stain was introduced subsequently.
To assess the efficacy of MUFP staining by comparing the quality of MUFP stain with conventional PAP stain.
FNAC procedure was performed by using 10 ml disposable syringe and 22-23 G needle. Total 131 FNAC cases were studied which were lymph node (30), thyroid (38), breast (22), skin and soft tissue (24), salivary gland (11) and visceral organs (6). Two smears were prepared and stained by MUFP and conventional PAP stain. Scores were given on four parameters: background of smears, overall staining pattern, cell morphology and nuclear staining. Quality Index (QI) was calculated from ratio of total score achieved to maximum score possible. Statistical analysis using chi square test was applied to each of the four parameters before obtaining the QI in both stains. Students t-test was applied to evaluate the efficacy of MUFP in comparison with conventional PAP stain.
The QI of MUFP for thyroid, breast, lymph node, skin and soft tissue, salivary gland and visceral organs was 0.89, 0.85, 0.89, 0.83, 0.92, and 0.78 respectively. Compared to conventional PAP stain QI of MUFP smears was better in all except visceral organ cases and was statistically significant. MUFP showed clear red blood cell background, transparent cytoplasm and crisp nuclear features.
MUFP is fast, reliable and can be done with locally available reagents with unequivocal morphology which is the need of the hour for a cytopathology set-up.
对细针穿刺细胞学检查(FNAC)评估的最短周转时间的需求促使染色技术不断创新,这些技术所需的染色时间更短且细胞形态明确。传统巴氏染色(PAP)的标准方案大约需要40分钟。为克服这一问题,引入了超快速巴氏染色(UFP),它将染色时间缩短至90秒,同时还提高了质量。然而,该方法所需的试剂不易获得,因此随后引入了改良超快速巴氏染色(MUFP)。
通过比较MUFP染色与传统PAP染色的质量来评估MUFP染色的效果。
使用10毫升一次性注射器和22-23G针头进行FNAC操作。共研究了131例FNAC病例,包括淋巴结(30例)、甲状腺(38例)、乳腺(22例)、皮肤和软组织(24例)、唾液腺(11例)和内脏器官(6例)。制备两张涂片,分别用MUFP和传统PAP染色。根据四个参数评分:涂片背景、整体染色模式、细胞形态和细胞核染色。质量指数(QI)通过将获得的总分与可能的最高分的比值计算得出。在计算两种染色的QI之前,对四个参数分别应用卡方检验进行统计分析。应用学生t检验评估MUFP与传统PAP染色相比的效果。
MUFP对甲状腺、乳腺、淋巴结、皮肤和软组织、唾液腺及内脏器官的QI分别为0.89、0.85、0.89、0.83、0.92和0.78。与传统PAP染色相比,除内脏器官病例外,MUFP涂片的QI在所有病例中均更好,且具有统计学意义。MUFP显示出清晰的红细胞背景、透明的细胞质和清晰的细胞核特征。
MUFP快速、可靠,可使用当地可得的试剂进行,细胞形态明确,这是细胞病理学设置当前所需。