K. Degitz, DETECTION OF MYCOBACTERIAL DNA IN THE SKIN - ETIOLOGIC INSIGHTS AND DIAGNOSTIC PERSPECTIVES, Archives of dermatology, 132(1), 1996, pp. 71-75
Background: Tuberculosis may be as old as mankind and continues to be
a serious medical problem today. Cutaneous tuberculosis shows consider
able morphological variability, and it is included in the differential
diagnosis of many other skin disorders. It is especially difficult to
distinguish skin tuberculosis from other granulomatous processes of t
he skin. Therefore, reliable laboratory tests are needed to confirm or
rule out the diagnosis. However, the diagnostic identification of Myc
obacterium tuberculosis and related organisms has remained difficult u
sing conventional laboratory tests (ie, microscopy and culture).Observ
ations: The diagnostic usefulness of molecular techniques, especially
the polymerase chain reaction (PCR), in skin tuberculosis is reviewed,
and the technical issues of PCR in general are discussed, with specia
l regard to the analysis of mycobacterial DNA in skin specimens. The P
CR has been successfully applied to detect DNA from M tuberculosis in
lupus vulgaris and several other forms of skin tuberculosis. It has al
so been used to identify mycobacterial DNA in certain forms of tubercu
lids, thereby supporting the long- and often-debated tuberculous origi
n of these skin disorders. Investigations of the presence of mycobacte
rial DNA in cutaneous sarcoidosis have not lent support to a general r
ole for mycobacteria in sarcoidosis. Conclusions: Polymerase chain rea
ction-based detection of M tuberculosis DNA in skin samples may extend
and improve the diagnostic panel for cutaneous tuberculosis, if the t
echnique is prudently and properly used. Furthermore, PCR provides exc
iting opportunities to gain further insight into the pathogenesis of c
utaneous tuberculosis and other granulomatous skin diseases.