Amniotic Band Syndrome (Streeter Dysplasia)

Updated: Sep 07, 2022
  • Author: Twee T Do, MD; Chief Editor: Jeffrey D Thomson, MD  more...
  • Print
Overview

Practice Essentials

Streeter dysplasia is a term that historically has been used to describe a complex disorder characterized by constricting rings, acrosyndactyly, or, often, amputations of the extremities of neonates. It is analogous to constriction band syndrome or amniotic band syndrome (ABS; also referred to as amniotic band sequence [1] ), which was recognized as early as 300 BCE.

Depending on the severity of the constriction, the defect may be as minimal as a merely cosmetic band. Deeper bands may cause lymphatic obstruction leading to edema and vascular compromise that necessitates immediate release. Pressure from the bands may potentially cause abnormalities distal to the constriction, such as hemihypertrophy, anterolateral bowing, pseudarthrosis, leg-length discrepancy, and resistant teratologic clubfeet. These conditions may lead to limited function and difficulty with ambulation. [2, 3, 4]

Constriction bands across the head and face may lead to facial clefts. If the cleft extends into the cranium, encephaloceles may result. Bands that cross the body may compromise the chest (thoracoschisis or extrathoracic heart) or abdomen (gastroschisis).

Because ABS is an intrauterine phenomenon probably caused by the rupture of amniotic membranes and constriction of the developing tissue, no medical treatment exists for the condition. (See Treatment.) Indications for intervention depend on the medical stability of the child and on the neurovascular status of the limb. Anencephaly usually is incompatible with life, but the other deformities can be triaged for correction and reconstruction. Of all the deformities, only the tight constriction bands with gross lymphedema, vascular compromise, or both necessitate immediate surgical release.

Next:

Anatomy

The anatomy relevant to surgery for ABS depends on the area of the body affected. Most bands are superficial, and only the skin and subcutaneous tissue are involved. However, the neurovascular bundle may be displaced near areas of banding. Therefore, this possibility must be taken into consideration with dissection for excision in order to avoid devascularization or denervation of the involved body segments.

Previous
Next:

Pathophysiology

The developing embryo sits within two cavities, the amnion and the chorion. As development occurs, the amnion presses against the extracoelomic space, eventually obliterating it and bringing the amnion up to and supported by the chorion. This phenomenon occurs on or about week 12 of gestation. Incomplete obliteration of the extracoelomic space renders the amnion fragile and subject to spontaneous or traumatic rupture. [5] After the rupture, a transient oligohydramnios occurs due to extravasation of amniotic fluid. Until the chorion adjusts to the permeability, the developing fetus has very little room in which to move. This may contribute to the severity of clubfeet deformities seen with ABS.

This decrease in space also allows the resultant floating amniotic bands to easily ensnare a developing body part. Early in gestation, the encircling bands may result in spontaneous abortions. If the constriction occurs after development is nearly complete, only fissures, acrosyndactylization, and intrauterine amputation are noted on the extremities as typical manifestations. If the amniotic bands are swallowed while still partially attached to the placenta, the tether may lead to bizarre facial clefts and palate deficiencies. [6]

Previous
Next:

Etiology

Two main lines of thought have been followed regarding the etiology of ABS, attributing the condition either to intrinsic or to extrinsic causes.

Hippocrates suggested that extrinsic pressures from a ruptured amniotic membrane lead to the formation of bands or digital amputations. In 1652, van Helmont reported on intrauterine amputations, which he attributed to the pregnant mothers having looked upon maimed soldiers. Montgomery [7] in 1832 and Simpson [8] in 1836 subsequently described series of amniotic band–associated deformities and discussed the differences between agenesis-induced and amniotic band–induced amputations.

The condition was not referred to as Streeter dysplasia until 1930, when Streeter postulated a germ plasm defect as one plausible etiology. [9] At that time, this theory was well accepted because of the associated anomalies, which occurred far from the site of the constriction bands. Streeter proposed that a disruptive event occurs during blastogenesis, leading to an intrinsic germ plasm defect. This causes the soft tissue to slough. External healing of the slough leads to the constricting rings and the resultant localized developmental defects.

Cases of ABS in which the amnion is intact supported Streeter's theory, as did the frequently associated renal abnormalities (37% of cases) and occasional cardiac abnormalities. Ainhum, a predominantly African syndrome in which progressive circumferential ulceration leads to eventual amputation of digits, is an inherited disease, lending further support to an intrinsic developmental defect as a cause of digit amputation. Streeter aggressively defended this theory for more than 35 years. For his long and avid support, many surgeons still describe this disorder as Streeter dysplasia.

In 1960, Patterson used histology to show how constriction bands look like normal skin creases. He hypothesized that the same lack of mesodermal development occurs in the area of the band, thereby making the bands simply abnormal creases. [10]

Patterson's theory was later refuted by Torpin, who examined many placentae and infants with the disorder. [11] In 1965, Torpin reintroduced the extrinsic theory originally held by Hippocrates. He proposed that maternal trauma leads to rupture of the amniotic membrane, which then forms into strands. These encircling strands cause extrinsic compression on the head or limb, leading to the formation of bands, vascular occlusion, and, eventually, amputations. This came to be the most widely supported hypothesis; therefore, ABS would be a more accurate name for this disorder than Streeter dysplasia.

The lack of family history or predictable recurrences in families of children born with ABS militated against the theory of an inherent or genetic component to the condition. Zionts et al [12] were able to demonstrate variable findings of the syndrome in monozygotic twins who each were affected by amniotic bands. These and other sporadic findings were more consistent with the view that external compression is the etiologic root of this syndrome. [13]

A sonographic study by Barzilay et al suggested that prior uterine surgery may be a risk factor for ABS. [14]

Previous
Next:

Epidemiology

The estimated frequency of ABS in the United States is 1 per 3000 pregnancies (if the potential miscarriages that occur from severe banding early in gestation are considered). More common statistics show an incidence of 1 case per 10,000-15,000 population. One of the few epidemiologic studies was a 1988 study from Atlanta that cited the incidence as 1.16 cases per 10,000 population. No sex predilection is recognized.

The incidence overseas is similar to that in the United States. The birth defect registry of Western Australia cited an incidence of 1.15 per 10,000 population.

Previous
Next:

Prognosis

The prognosis for patients with isolated superficial extremity bands is good (see the image below). Aside from cosmetic variability, no functional deficits remain.

Image shows the lower limb of a young child born w Image shows the lower limb of a young child born with moderate bands that extend deep to the fascia but do not compromise the neurovascular system.

Deeper bands may be associated with progressive problems leading to later lymphatic and neurovascular compromise that necessitates surgical intervention. For patients with acrosyndactyly, hand function is limited secondary to stiffness of the joints, but good prehension and grasp may be obtained with reconstructive procedures. Children who have had intrauterine amputations are usually well adapted to their physical limitations, and often little needs to be done. In children with a transverse deficiency proximal to the ankle joint, a prosthesis is required for full function.

Previous