Background: Acid-fast staining for the detection of Mycobacterium tuberculosis has a high false negative-rate, partly due to it is hard to get a good positive control tissue of acid-fast staining. We aimed to design a simple and convenient method for making positive quality controls for acid-fast staining in paraffin-embedded sections.Methods: Three methods were used to get more tuberculous bacteria, which involving centrifugation, mixing, and culture of tubercle bacilli in pleural fluid, prior to the preparation of paraffin-embedded sections.Results: Culturing tubercle bacilli in pleural fluid proved to be, by far, the best of the three methods, with sufficient bacteria, convenient observation, clear staining, and potential for upscaled production.Conclusions: The application of this method should improve the detection rate of tuberculous bacteria, thus facilitating clinical treatment.

ABSTRACT:We identified an unusual novel nonsense mutation in exon 3 of the androgen receptor (AR) gene in a patient with complete androgen insensitivity that was persistence of Wolffian derivatives. Sequence analysis revealed a substitution (CRT) at position 2211 and a deletion of G at position 2213 in exon 3 of the AR gene, resulting in the conversion of arginine (CGG) to a stop codon (TGA) of the AR. Western blotting demonstrated a truncated AR with around 70 kd was expressed. Histology of patient's testes showed that seminiferous tubules were totally filled with Sertoli cells without germ cells. Immunohistochemistry revealed positive AR localization in the nuclei of Sertoli cells and epithelia of efferent ductule and vas deferens. AR immunoexpression was stronger in the epithelia of efferent ductule and vas deferens than in Sertoli cells. The study extends the spectrum of exon 3 mutations in the AR gene.