Objective
To assess the distribution and type of nerve fibers present in human perito
neal adhesions and to relate data on location and size of nerves with estim
ated age and with clinical parameters such as reports of chronic pelvic pai
n.
Summary Background Data
Peritoneal adhesions are implicated in the cause of chronic abdominopelvic
pain, and many patients are relieved of their symptoms after adhesiolysis.
Adhesions are thought to cause pain indirectly by restricting organ motion,
thus stretching and pulling smooth muscle of adjacent viscera or the abdom
inal wall. However, in mapping studies using microlaparoscopic techniques,
80% of patients with pelvic adhesions reported tenderness when these struct
ures were probed, an observation suggesting that adhesions themselves are c
apable of generating pain stimuli.
Methods
Human peritoneal adhesions were collected from 25 patients undergoing lapar
otomy, 20 of whom reported chronic pelvic pain. Tissue samples were prepare
d for histologic, immunohistochemical, and ultrastructural analysis. Nerve
fibers were characterized using antibodies against several neuronal markers
, including those expressed by sensory nerve fibers. In addition, the distr
ibution of nerve fibers, their orientation, and their association with bloo
d vessels Were Investigated by acetylcholinesterase histochemistry and dual
immunolocalization.
Results
Nerve fibers, identified histologically, ultrastructurally, and immunohisto
chemically, were present in all the peritoneal adhesions examined. The loca
tion of the adhesion, its size, and its estimated age did not influence the
type of nerve fibers found. Further, fibers expressing the sensory neurona
l markers calcitonin gene-related protein and substance P were present in a
ll adhesions irrespective of reports of chronic abdominopelvic pain. The ne
rves comprised both myelinated and nonmyelinated axons and were often, but
not invariably, associated with blood vessels.
Conclusions
This study provides the first direct evidence for the presence of sensory n
erve fibers in human peritoneal adhesions, suggesting that these structures
may be capable of conducting pain after appropriate stimulation.