The authors report two cases of actinomycosis in children: one thoraci
c and the other retroperitoneal. They emphasize the difficulties of di
agnosis before the stage of parietal extension with cutaneous fistula
and characteristic yellow granular discharge. These difficulties are d
ue to: The rarity of visceral actinomycosis, particularly in children.
The lesion has a similar appearance to that of a tumor; an extensive
pre-operative work-up is mandatory (ultrasound, computed tomogram scan
, repeated ultrasound-guided needle biopsy), although this work-up may
not necessarily lead to the correct diagnosis. A surgical biopsy will
often confirm the diagnosis, provided the diagnosis has been previous
ly considered. The necessity of using very specific tests for correct
identification of the organism. Therefore, in a case of pseudo-inflamm
atory pseudotumor, visceral actinomycosis must be considered in order
to guide microbiological and pathological studies, although this diagn
osis is rare. Once the diagnosis has been made, prolonged treatment wi
th penicillin is effective and complete recovery is generally obtained
.