Introduction
In 1908, TS Cullen classified adenomyosis into three distinctive
subtypes of adenomyosis based on morphologic appearances [1]. He
described:
(i) smooth enlargement of the uterus without disturbing its contour,
(SS, type 1 or type 3, AM)
(ii) subperitoneal or intraligamentary adenomyomata, (SS, type 4, AM)
(iii) submucous adenomyomata. (SS, type 3, AM)
It is now clear to us in Shanghai, that there are two, common
patterns of adenomyosis in China that are relatively unusual in Western
countries though TS Cullen illustrated both types in his book under
the category “smooth enlargement of the uterus without disturbing its
contour” [2]. The most distinctive is diffuse, symmetric, adenomyosis
that usually presents as a painless mass (250-1250g) with symptoms of
“pressure” on adjacent organs. "Shanghai system" (SS), Type 1, AM,).
Histologic examination shows there is no evidence of nerves anywhere
in either the uterus, or Fallopian tubes [2] (Figure 1A-F). In a second,
common, clinical presentation in Shanghai, there may be extreme
enlargement of a focal posterior wall adenomyoma that produces
marked distortion of the uterine cavity, asymmetry of the uterus, and
often, uterine retroversion (Figure 3E-F , type 3, AM, SS). The clinical
presentation is also usually painless, with some asymmetry of the
uterosacral ligaments, and, on histologic examination there are no
nerves in the myoma. Both are relatively rare presentations in UK or
US gynecology.
The best evidence in the US literature for the etiology of
adenomyosis derives from the observation that vigorous curettage of
one horn of the uterus of a pregnant rabbit produces adenomyosis,
whilst allowing the pregnancy to continue in the opposite horn [3]. This
is the “trauma” hypothesis which is reinforced by radiologic interest in
the width of the endometrial- myometrial interface (or, junctional zone
(JZ) of the uterus). Twelve millimeter thickness of the JZ guarantees
a histologic diagnosis of adenomyosis though others discuss different
degrees of sensitivity and specificity at different thicknesses [4,5]. These
radiologic colleagues, however, make no mention of the endometrial-
myometrial nerve plexus described by Krantz [6] that postdates many
of the classic descriptions of adenomyosis in the US literature [3,7], and
is not mentioned in more recent updates [8,9]. If there is interruption
of this nerve plexus either by direct trauma at curettage, or, through
uterine tachysystole, or, through injuries to the uterotubal nerves that
pass through the uterosacral ligaments to supply it, then each may
contribute to loss of innervation in different parts of the uterus and
Fallopian tubes. Tubal ligation and Cesarean section have both been
discussed in the context of the etiology of adenomyosis. Tubal ligation
may increase intrauterine pressures at different times of the menstrual
cycle [10] whereas a myometrial incision (above the lower segment of
Lin Na Z (2019) Neuro-etiologic classification of adenomyosis: the “Shanghai system”
Clin Obstet Gynecol Reprod Med, 2019 doi: 10.15761/COGRM.1000260
Volume 5: 2-6
the uterus) may injure endometrial-myometrial nerves, or, tearing one,
or both, angles of the uterine incision may do the same ? [11] Some
series of US patients refer to uterine weights of greater than 250g with
the highest recorded weight of 705 g but they are rare [3]. Typically,
US women present with painful periods that require hysterectomy
at uterine weights of 80-150g (type 2, AM, SS) that are common in
Western clinical practice, though not mentioned in Cullen’s original
account. They is no published evidence for significant numbers of cases
of diffuse, painless adenomyosis (SS, type 1, AM) and focal, painless
adenomyosis (SS, type 3, AM), that we frequently observe in Shanghai ?
The nerve supply of the uterus
As undergraduates we saw cadaveric material preserved in
formalin (that destroys autonomic nerves) whereas Lee used alcohol
in his dissections [12,13]. In an alcohol-embalmed cadaver the full
morphology of the pelvic plexi is clear [14] as the nerves pass through
the fan of the uterosacral-cardinal ligament plexus to converge on the
vaginal vault where they are susceptible to injury through difficult
first labors, physical efforts during defaecation, and, complications
of the management of evacuation of the uterus through surgical and
medical techniques [15]. Partial, or complete, injuries to the uterosacral
ligaments results in partial, or complete, injuries to the uterotubal
nerves with differing degrees of aberrant reinnervation depending
on the extent of the injury [15]. The distal third of the Fallopian tubes
receives nerve supply from the ovarian plexus through the free edge of
the mesosalpinx [16].
In this discussion it is both the intrauterine, and extrauterine,
nerve supply that assumes significance in relation to different patterns
of adenomyosis. Within the uterus mixed nerve bundles delivered (a)
in the uterosacral ligaments, and, (b) along with the uterine artery,
form the endometrial-myometrial nerve plexus and subserosal nerve
plexus, respectively, that reflects the differing embryologic origins of
the endometrium and myometrium [6,17]. Both deliver sparse nerve
bundles to the myometrium though normal endometrium does not
carry a nerve supply. Intra-uterine injuries to the nerve supply will
cause collateral sprouting of nerve bundles and aberrant reinnervation
of injured nerves (Figure 2C-D) whereas pre-uterine injuries to nerves
in the uterosacral ligaments may demonstrate loss of nerves in adjacent
nerve bundles (Figure 3C-D). The two patterns of injury are separate
and distinctive.
Figure 1(A-F). Type 1, diffuse, symmetric, painless adenomyosis. (A) Diffuse, symmetric
adenomyosis at uterine weight of 260g. (B) Complete absence of uterosacral ligaments at
laparoscopy. (C) Complete loss of the endometrial-myometrial nerve plexus (anti-S100,
x100). (D) Complete loss of uterotubal nerves throughout the resected specimen. (E)
Diffuse, symmetric adenomyosis (T2 weighted, MR scan, LS). (F) Diffuse, symmetric
adenomyosis (T2 weighted, MR scan, TS).
Figure 2(A-F). Type 2, irregular, asymmetric, painful adenomyosis. (A) Irregular,
asymmetric, painful in uterus weighing less than 150g. (B) Irregular scarring of uterosacral
ligaments at laparoscopy. (C) Aberrant reinnervation of endometrial-myometrial interface
(anti-S100, x 100). (D) Aberrant reinnervation in the uterosacral ligaments (anti-S100,
x100). (E) Irregular, asymmetric adenomyosis with enlarged cervix and Cesarean scar on
the anterior uterine wall (T2, weighted MR scan, LS). (F) High signal intensity of injured
uterosacral ligaments on either side of the cervix (T2 weighted, MR scan, coronal section)
Lin Na Z (2019) Neuro-etiologic classification of adenomyosis: the “Shanghai system”
Clin Obstet Gynecol Reprod Med, 2019 doi: 10.15761/COGRM.1000260
Volume 5: 3-6
Previous classifications of adenomyosis
A number of classifications of the varying clinical phenotypes
of adenomyosis have been set out. KF von Rokitansky identified the
condition in 1860 with one of the original, light microscopes [18]
though it was TS Cullen (1908) who presented the first classification of
adenomyosis based largely on macroscopic and microscopic studies of
the condition [1]. John Sampson (1921) discussed a similar classification
to that of TS Cullen [19]. More recently, there have been two clinical
contributions to attempt to improve the classification of adenomyosis;
Dr Kishi (KS) in Takanohara Hospital, Nara, Japan discussed four
subtypes of adenomyosis based on magnetic resonance imaging [20],
and, Dr. Bazot (BZ), at Tenon Hospital, Paris, who described three
different patterns of adenomyosis using vaginal sonography and MR
imaging [21]. There are some minor differences between the two
classifications but both are based on specific, radiologic appearances
(Table 1).
The “Kishi” classification, 2012 (Table 1A)
In 152 women undergoing MRI, Kishi [20] described four subtypes
of adenomyosis (Table 1A). In their stepwise regression analysis, Kishi
et al. noted that a significant proportion of type 1 adenomyosis (KS
1) had prior terminations of pregnancy whereas type 2 (KS 2) did not
(32.2% v 7.8%), they proposed that a “barrier” exists at the endometrial-
myometrial interface which prevents adenomyosis, and, this barrier
may be injured by pregnancy or curettage. In type 3 adenomyosis
(KS 3), clinical features included menorrhagia (18/22, 81.8%) and
dysmenorrhea (18/22, 81.8%). They suggested that this is a “de novo
product” of embryologic or metaplastic origin. In type 4 adenomyosis
(KS 4) this was a heterogeneous group where the adenomyosis was
so “widely extended and expanded that the relationship with uterine
structural components could not be clearly evaluated” . The authors
conclude that this subgroup is a heterogeneous mix of types 1-3
adenomyosis (KS 1-3). In their discussion, they draw attention to the
fact that type 3 adenomyosis (KS 3), was the youngest group of women
(34 v 38 years), and, to the paradox that some women in each group
were symptomatic, though others were asymptomatic.
The “Bazot” classification, 2018 (Table 1B)
Bazot recognizes three types of adenomyosis [21]. He draws
attention to the classification by John Sampson (1921) which he
replicates with this MRI classification [19]. He draws distinctions
between what ultrasound examination can do, and, how MR imaging
adds to the ultrasound observations. Interestingly, Bazot distinguishes
11 patterns of adenomyosis on MR imaging, most are recognizable
variations of his three main groups (BZ 1-3) but two relate to adjacent
injuries to the subserosal uterine plexus, and, bladder or rectum. These
imply significant intrapartum injuries to adjacent organs though these
are not discussed in detail.
The "Shanghai system" of classification (Table 2)
For a variety of reasons, we offer a third classification of adenomyosis
based on clinical, laparoscopic, histologic and radiologic appearances
that define the clinical anatomy and histologic injuries carefully (SS
types 1-4, AM; Table 2).
(a) we noticed clear differences in incidence of some patterns of
adenomyosis in China compared to Europe.
(b) we observed some unusual neurologic injuries to the uterine nerve
supply in different patterns of adenomyosis
(c) we noted limited awareness of the nerve supply of the uterus, and,
different lesions of adenomyosis appears to “map” very precisely to
the anatomic sites of the two key, uterine nerve plexi (endometrial-
myometrial interface and subserosa)
(d) in this classification there are four types of adenomyosis (SS,
types 1-4, AM) with types 1-3 associated with precise neurologic
injuries.
Type 1 AM, Diffuse, symmetric, painless adenomyosis
(SS type 1, AM Figure 2A-F)
In our initial series of 34/34 women with diffuse, symmetric,
painless adenomyosis, these women had no uterosacral ligaments
(P<0.001), no nerves at the endometrial-myometrial nerve plexus
(P<0.001), and, no nerves in their uteri or Fallopian tubes (P<0.001)
compared to controls [2]. Either the injury to uterotubal nerves came
first, or, the enlargement of the uterus destroyed the nerves during the
enlarging process. We prefer the former explanation since:
(a) all these women had, at least one, second trimester abortion,
(which can avulse both uterosacral ligaments in nulliparous
women)
(b) there are no nerves of any kind at the endometrial-myometrial
nerve plexus which is continuous with the nerves in the uterosacral
ligaments
(c) all uteri in this series had similar histology of uterus, uterosacral
ligaments and Fallopian tubes, and weighed between 260g and
1160g,
(d) no woman complained of pain; the worst symptoms being
“heaviness” with “pressure” on bladder and bowel leading to
frequency passing urine, and, constipation.
We believe this pattern of adenomyosis results from complete loss
of the nerve supply at the endometrial-myometrial interface owing
to significant tractino being applied to the cervix (and uterosacral
ligaments) during second trimester abortions that results in complete
avulsions of the uterosacral ligaments. Second trimester abortions are
relatively common in China, though unusual in UK clinical practice
where most procedures take place during the first trimester of
pregnancy, often using medical treatment.
Type 2 AM, asymmetric, painful adenomyosis (SS type
2, AM; Figure 2A-F)
In this second pattern of adenomyosis, there is aberrant
reinnervation in the myometrium in association with asymmetric,
painful, adenomyosis associated with the endometrial-myometrial
interface (SS 2, type 2 adenomyosis, Figure 2A-F). These often occur
in association with collateral sprouting of nerve bundles that is
pathognomonic of prior traumatic injury (Figure 2C-D). In many cases
we find evidence of over-vigorous uterine curettage, difficult vaginal
delivery, or, excessive uterine activity associated with administration of
oxytocin, prostaglandins or misoprostol – drugs that were not available
to TS Cullen in 1908 or JR Sampson in 1921. The injury is largely
confined to the body of the uterus and the clinical presentation often
includes irregular, painful bleeding at reduced uterine weights (80-
150g) that regularly results in hysterectomy.
There are two patterns of neural injury caused by, at least, two
different patterns of trauma, in type 2, AM. Firstly, there is a degree
Lin Na Z (2019) Neuro-etiologic classification of adenomyosis: the “Shanghai system”
Clin Obstet Gynecol Reprod Med, 2019 doi: 10.15761/COGRM.1000260
Volume 5: 4-6
1. Intrinsic adenomyosis that develops in direct connection with a thickened junctional zone (JZ) (KS, type 1, AM)
2. Extrinsic adenomyosis that develops in the outer shell of the myometrium and the junctional zone was intact (KS, type 2, AM)
3. Intramural adenomyosis which develops without relationship to the JZ or the subserosal layers (KS, type 3, AM)
4. Indeterminate adenomyosis that develops outside of the three prior subtypes (KS type 4, AM)
Table 1A. The “Kishi” classification of adenomyosis. It is based on stepwise, logistic regression analysis of 152, surgically-treated cases of adenomyosis and published as Kishi Y ,
Suginami H, Kuramori R et al. “Four subtypes of adenomyosis assessed by magnetic resonance imaging and their specification.” Am J Obstet Gynecol 2012; 207: 114 e1-7
1. Internal adenomyosis (BZ, type 1, AM)
Diffuse, symmetric or asymmetric widening of myometrium secondary to myometrial hypertrophy with thickening of the junctional zone, often with concurrent leiomyomas
2. External adenomyosis (BZ, type 2, AM)
Arises in the outer part of the uterus disrupting the subserosa but not affecting the JZ, often associated with “deep” endometriosis. It can be found with internal adenomyosis or
adenomyomas.
3. Adenomyomas (BZ, type 3, AM)
An adenomyoma is an ill-defined, myometrial mass containing high-intensity, central cystic areas. Neither JZ or subserosa are affected by the presence of isolated adenomyoma
Table 1B. The “Bazot” classification of adenomyosis. It is based on a descriptive evaluation of transvaginal sonography and magnetic resonance imaging descriptions of adenomyosis
resulted in three categories of adenomyosis with eleven anatomic, MRI descriptions, published as M. Bazot, E Darai. “Role of transvaginal sonography and magnetic resoanance imaging
in the diagnosis of uterine adenomyosis” Fertil Steril 2018; 109(3) 389-397
Type 1 Diffuse, symmetric, painless adenomyosis (SS, type 1, AM; Figure 2)
This pattern of adenomyosis typically presents as a painless pelvic mass in a parous woman in her mid-forties with a prior history of one, or more, previous first or second trimester
abortions. At laparoscopy there is no evidence of uterosacral ligaments. Histologically there are no nerves in the uterus or Fallopian tubes, particularly there are no nerves at the site of the
endometrial-myometrial nerve plexus (JZ). MR imaging shows symmetrical enlargement of the uterus, with accompanying enlargement of the cervix.
Type 2 Irregular, asymmetric, painful adenomyosis (SS, type 2, AM; Figure 3)
This pattern of adenomyosis typically presents with heavy painful, menstrual bleeding in a parous woman in her fifth decade. Typically, there is evidence of injuries to the uterosacral
ligaments with scarring of their uterine insertions. Histologically there is aberrant reinnervation in the body of the uterus associated with the endometrial-myometrial interface (JZ). MR
imaging shows an irregular, asymmetric pattern of adenomyosis centred on the endometrial-myometrial interface. The uterine cervix may be enlarged owing to accompanying injuries to
its nerve supply.
Type 3 Focal painless adenomyoma (SS type 3, AM; Figure 4)
This pattern of adenomyosis is typically asymptomatic unless associated with other forms of “endometriosis”. Typically, its “maps” to the two main nerve plexi in the uteri i.e. the
endometrial-myometrial nerve plexus, or, the subserosal nerve plexus, or, their myometrial branches. MR imaging shows a focal, high signal intensity, “adenomyoma”. The uterine cervix
is usually not enlarged as there has been no injury to its nerve supply. These adenomyomas can be very large and appear irregular because they are “compressed” between intact, subserosal
and endometrial-myometrial nerve plexi.
Type 4 Painless intraligamentary adenomyosis (SS type 4, AM)
There are a group of other sources of adenomyosis – some are of embryological origin, others are pedunculated, others form atypical adenomyomatoid polyps, that require a separate
category. They are rare, and, usually distinguishable from more traditional patterns of adenomyosis.
Table 2. The "Shanghai system" of classification of adenomyosis. This system relies on clinical, laparoscopic, histologic and radiologic features of adenomyosis to produce a neuro-
aetiologic classification. Each pattern of adenomyosis arises from an injury to the uterine supply that varies with the site, nature and extent of the injury; (A) complete avulsion of
the uterosacral ligaments leads to diffuse, symmetric, painless adenomyosis (type 1), (B) excessive traction to the cervix (less than that necessary to produce avulsion) combined with
overvigorous curettage of the endometrium, or, excessive uterine activity, leads to irregular, asymmetric, painful adenomyosis (type 2, AM), (C) partial, pre-uterine injury to a few nerves in
either uterosacral ligament leads to endometrial or myometrial hyperplasia and development of focal, painless, myoma
of traction to the cervix that is not sufficient to completely avulse
the uterosacral ligaments, but, allows them to reattach to the lower
uterus and cervix as scarring (Figure 2B) that enables a “bridge”
for reinnervation of the lower uterus (Figure 2D). Over-vigorous
curettage at the same procedure causes a direct injury to the
endometrial-myometrial interface creating aberrant reinnervation at
the endometrial-myometrial interface (Figure 2C) with subsequent,
marked dysmenorrhea that often necessitates an early hysterectomy
at low uterine weights (80-150g) [3]. Both of these specific injuries
may also result from trauma during vaginal delivery; typically uterine
tachsystole replicates the partial injury to the endometrial-myometrial
interface whereas big babies (>4000g), malpresentations, and, operative
vaginal deliveries may all contribute to injuries to the insertions of the
uterosacral ligaments and their, contained uterotubal nerves [22].
Type 3 AM, painful or painless, adenomyomas, (SS type
3, AM; Figure 3A-F)
In the third pattern of adenomyosis, there is a circumscribed
tumor that often “maps” to either the anatomic position of the
endometrial-myometrial or subserosal nerve plexi, or, most commonly
the posterosuperior myometrium of the uterus. Histologically, there is
loss of nerve fibers in myometrial nerve bundles adjacent to painless
adenomyomas and leiomyomas (SS 3, Type 3 AM), often with large
numbers of narrowed arterioles adjacent to the tumor. We believe
these tumors arise from pre-uterine neural injuries because there is no
evidence of collateral sprouting in these nerve bundles implying that a
focal, pre-uterine injury to the nerve bundle had taken place resulting
in loss of specific, nerve fibers (Figure 3C-D). Sometimes it is possible
to discern an injury to the uterosacral ligament, or, there is a deposit of
ectopic endometrium to mark the underlying injury (Figure 3B).
This injury takes place as part of a first trimester abortion
procedure when paracervical infiltration of local anesthesia creates
the conditions for injuries to individual nerve fibers, particularly those
in the superior quadrants of paracervical tissue. Injuries to individual
nerve fibers in the uterosacral ligaments create neurologic deficits in
the myometrium leading to focal hyperplasia, and, formation of an
adenomyoma or leiomyoma. We do not understand the difference
between the etiology of the two tumors as yet?
Type 4, painless, intraligamentary adenomyoma (SS
type 4, AM)
TS Cullen was aware of this least common pattern of adenomyosis
though we are aware there are also adenomyomatous patterns of uterine
polyp, and, pedunculated forms of adenomyosis that appear to have a
non-neurologic origin.
Lin Na Z (2019) Neuro-etiologic classification of adenomyosis: the “Shanghai system”
Clin Obstet Gynecol Reprod Med, 2019 doi: 10.15761/COGRM.1000260
Volume 5: 5-6
plexus that enters the uterus with the uterine artery [6,17]. Leyendecker
has been a proponent of the importance of prior tissue injury in the
“endometriosis-adenomyosis” spectrum and has emphasized his
observation of 11 cases of “cornual” adenomyotic cysts as a rare but
distinctive form of adenomyosis [23,24]. In the “Shanghai system” , these
Result
from an unusual injury to the uterine nerve supply at the anterior
border of the uterosacral ligament (SS, type 3, AM; Figure 2B). In this
account, these injuries to the anterior border of the uteosacral ligament
are likely to result from paracervical infiltration with lignocaine
followed by traction to the cervix, that contributes to focal tearing of
pre-uterine, nerve fibers with subsequent development of a myoma.
There may be other reasons.
The increased frequency of the diffuse, symmetric, “painless”
pattern of adenomyosis in China raises a number of important aetiologic
questions. Firstly, it appears that 1000g of “ectopic” endometrium can
occupy a woman’s pelvis without any discomfort to her. Secondly,
excessive traction to the cervix during any gynecologic procedure may
avulse one, or more, nerve bundles creating the conditions for all three
types of adenomyosis (SS, types 1-3, AM). Thirdly, the apparent absence
of SS, type 2, AM in the Cullen and Sampson classifications raises the
concern that the injury to the endometrial-myometrial interface, or,
“junctional zone” is often a contemporary, iatrogenic injury associated
with uterotonic agents such as oxytocin, prostaglandins or misoprostol,
leading to injury to the endometrial-myometrial nerve plexus [1,19].
Some patterns of adenomyosis may be preventable by improved
management of labour, and, evacuation of the uterus. Active measures
to prevent excessive uterine activity with oxytocin, prostaglandins and
misoprostol need more emphasis. There is no reason for excessive
traction to the cervix if the surgeon understands there are large numbers
of delicate nerve bundles associated with its posterior surface.
All three, benign, gynecologic pathologies (endometriosis,
adenomyosis, leiomyoma) carry injuries to the uterine nerve supply [26-
32]. In this classification we propose that three patterns of adenomyosis
Figure 4(A-D). Patterns of injury to the uterosacral ligaments in different patterns of
adenomyosis. (A) Normal uterosacral ligaments with peritoneal window associated with
right, uterosacral ligament have nerves running through them that converge on the cervix.
(B) Bilateral avulsions of uterosacral ligaments cause diffuse, symmetric adenomyosis (SS,
type 1, AM, Fig. 1a-f). (C) Bilateral scarring of uterosacral ligaments at uterine insertions &
over-vigorous curettage of the endometrial cavity cause irregular painful, adenomyosis (SS,
type 2, AM, Fig. 2a-f). (D) Discrete injuries to the nerves running through the uterosacral
ligaments associated with paracervical infiltration of anesthetic agents result in focal,
painless adenomyoma (SS, type 3, AM, Fig 3a-f).
Figure 3(A-F). Type 3, focal, painless adenomyoma. (A) Small, (1-2 cm diameter)
leiomyoma does not compress adjacent histologic features. (B) Focal injury, marked by
ectopic endometrium, at anterior border of uterosacral ligament. (C) Loss of nerve fibers
in a myometrial nerve bundle beneath the myoma (LS, anti-S100, x100). (D) Loss of nerve
fibers in a myometrial nerve bundle beneath the myoma (TS, anti-S100, x100). (E) Focal,
low intensity signal of a myoma on posterior wall of uterus (T2 weighted, MR scan, LS).
(F) Focal, low intensity signal of a myoma on posterior wall of uterus (T2 weighted, MR
scan, TS)
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