Peritoneal adhesions are a major complication of healing following surgery
or infection and can lead to conditions such as intestinal obstruction, inf
ertility, and chronic pain. Mature adhesions are the result of aberrant per
itoneal healing and historically have been thought to consist of non-functi
onal scar tissue. The aim of the present study was to analyse the cellular
composition, vascularity, and extracellular matrix distribution of human pe
ritoneal adhesions, to determine whether adhesions represent redundant scar
tissue or are dynamic regenerating structures. Furthermore, the histologic
al appearance of each adhesion was correlated with the clinical history of
the patient, to determine whether maturity or intraperitoneal pathology inf
luences adhesion structure. Human peritoneal adhesions were collected from
29 patients undergoing laparotomy for various conditions and were prepared
for histology, immunocytochemistry, and transmission electron microscopy. A
ll adhesions were highly vascularized, containing well-developed arterioles
, venules, and capillaries. Nerve fibres, with both myelinated and non-myel
inated axons, were present in adhesions from nearly two-thirds of the patie
nts, with increased incidence in those with a malignancy. Approximately one
-third of the adhesions contained conspicuous smooth muscle cell clusters l
ined by collagen fibres of heterogeneous size. Adipose tissue was a consist
ent feature of all the adhesions, with some areas displaying fibrosis, Ther
e appeared to be no correlation between the estimated maturity or site of e
ach adhesion and its histological appearance. However, intraperitoneal path
ology at the time of surgery did influence the incidence of some histologic
al features, such as the presence of nerve fibres, clusters of smooth muscl
e cells, and inflammation. This study challenges previous concepts that adh
esions represent non-functional scar tissue and clearly demonstrates that e
stablished adhesions are highly cellular, vascularized, and innervated, fea
tures more consistent with dynamic, regenerating structures. Copyright (C)
2000 John Wiley & Sons, Ltd.