TY - JOUR
T1 - Lumbosacral ectopic nephrogenic rest unassociated with spinal dysraphism
AU - Horenstein, Marcelo G.
AU - Manci, Elizabeth A.
AU - Walker, Andrew B.
AU - Dehner, Louis P.
PY - 2004/10/1
Y1 - 2004/10/1
N2 - Nephrogenic rests (NRs) are thought to originate from persistent nephrogenic blastema and are considered precursor lesions of Wilms' tumor (WT). These rests usually occur as perilobar and intralobar lesions in the kidney and, rarely, in ectopic sites. We report a midline lumbosacral ectopic NR in a healthy full-term newborn male with no family history of WT or WT-associated syndromes. The NR presented as a soft polypoid mass covered by normal skin. An MRI study revealed no lumbosacral spine abnormalities and no communication with the vertebral canal. The resected mass measured 3 cm and contained fat and had a central 1.2-cm solid nodule. The nodule was composed of blastema, epithelial elements (mature tubules and nephrons), and abundant stroma. No other somatic tissue elements were identified after complete microscopic examination. There are 4 cases of NRs reported in the lumbosacral area associated with spinal dysraphism, and only 2 cases, in addition to our report, unassociated with spinal abnormalities. The pathogenesis of heterotopic immature nephrogenic tissue remains a source of conjecture and speculation. If these lesions are heterotopic rests, their potential for neoplastic progression is probably quite limited, but if a monodermal teratoma, then more scrupulous clinical follow-up is warranted.
AB - Nephrogenic rests (NRs) are thought to originate from persistent nephrogenic blastema and are considered precursor lesions of Wilms' tumor (WT). These rests usually occur as perilobar and intralobar lesions in the kidney and, rarely, in ectopic sites. We report a midline lumbosacral ectopic NR in a healthy full-term newborn male with no family history of WT or WT-associated syndromes. The NR presented as a soft polypoid mass covered by normal skin. An MRI study revealed no lumbosacral spine abnormalities and no communication with the vertebral canal. The resected mass measured 3 cm and contained fat and had a central 1.2-cm solid nodule. The nodule was composed of blastema, epithelial elements (mature tubules and nephrons), and abundant stroma. No other somatic tissue elements were identified after complete microscopic examination. There are 4 cases of NRs reported in the lumbosacral area associated with spinal dysraphism, and only 2 cases, in addition to our report, unassociated with spinal abnormalities. The pathogenesis of heterotopic immature nephrogenic tissue remains a source of conjecture and speculation. If these lesions are heterotopic rests, their potential for neoplastic progression is probably quite limited, but if a monodermal teratoma, then more scrupulous clinical follow-up is warranted.
KW - Developmental abnormality
KW - Nephrogenic rest
KW - Sacrococcygeal teratoma
KW - Spinal dysraphism
KW - Wilms' tumor
UR - http://www.scopus.com/inward/record.url?scp=5044219583&partnerID=8YFLogxK
U2 - 10.1097/01.pas.0000131557.49774.29
DO - 10.1097/01.pas.0000131557.49774.29
M3 - Article
C2 - 15371957
AN - SCOPUS:5044219583
SN - 0147-5185
VL - 28
SP - 1389
EP - 1392
JO - American Journal of Surgical Pathology
JF - American Journal of Surgical Pathology
IS - 10
ER -