Introduction
Endometriosis is a condition in which endometrial-like glands
and stroma are located outside of the uterine cavity. The ectopic
endometrium is encountered most commonly pelvic structures
such as ovary, uterine ligaments, pelvic peritoneum, and genital
structures [1-4]. The usual site of endometriosis outside of the
abdominopelvic cavity is in or around the lung (intrathoracic cavity)
(Figure 1). Although endometriosis in general can affect up to 15%
of women of reproductive age, thoracic endometriosis remains
a very rare condition [5-9]. Thoracic endometriosis produces a
broad range of clinical and radiological manifestations, including
catamenial pneumothorax (80%), catamenial hemothorax (15%),
hemoptysis (5%), and rarely pulmonary nodules [5-9]. The age
of onset in patients with thoracic endometriosis (a mean of 35
years) is higher compared to a mean age at presentation of 25 to
30 years in patients with only pelvic endometriosis [5-9]. The exact
mechanism of catamenial pneumothorax associated with thoracic
endometriosis remains unclear, but several hypotheses have
developed to explain this condition.
Figure 1: Endometriosis involving the pleural surface of
diaphragm (arrows). The clinical and laboratory findings
have been reported previously [32].
ARTICLE INFO ABSTRACT
Received:
November 30, 2021
Published:
December 14, 2021
Citation: Shiomi Usida, Satoshi Ichigo, Hi-
roshi Takagi, Kazutoshi Matsunami, Tosh-
io Kasugai, Atsushi Imai. Pneumothorax
Associated with Thoracic Endometriosis:
Current Knowledge. Biomed J Sci & Tech
Res 40(3)-2021. BJSTR. MS.ID.006467.
Thoracic endometriosis is characterized by the presence of endometrial-like
glands and stroma within the lung parenchyma or on the diaphragm and pleural
surfaces. It remains unclear how endometrial tissue migrates into the thoracic
cavity and produces pneumothorax. Currently proposed hypotheses include
retrograde menstruation through diaphragmatic fenestrations, coelomic metaplasia,
prostaglandin, hematogenous or lymphatic metastases. None of the theories proposed
alone can elucidate all clinical manifestations of this condition, so the etiology of
the development of thoracic endometriosis is likely to be multifactorial and closely
intertwined with each other hypothesis.
Copyright@ Atsushi Imai | Biomed J Sci & Tech Res | BJSTR. MS.ID.006467.
Volume 40- Issue 3
DOI: 10.26717/BJSTR.2021.40.006467
32366
Retrograde Menstruation through Diaphragmatic
Fenestrations
The endometrial tissue is thought to move through the fallopian
tubes to the peritoneal cavity by retrograde menstruation backflow
[4]. The endometrial cells in peritoneal fluid may follow clockwise
peritoneal circulation and pass through the right paracolic gutter
towards the right sub-diaphragmatic region. The phrenicocolic
ligament on the left side and falciform ligament form barriers that
prevent cells and fluids from reaching the left sub-diaphragmatic
area [10,11]. Implantation of endometrial cell leads to the formation
of endometriotic nodules on the ventral side of the diaphragm [10].
The nodules cause cyclical necrosis and induce diaphragmatic
fragility, leading to the formation of the usual diaphragmatic
fenestrations. After endometrial tissue enters the pleural space, it
may form colonies in other part of the diaphragm or in the pleural
space. Air leaks from vagina may occur during the menstrual cycle
when the cervical mucus plug is deleted [10-14]. This hypothesis
may be in good agreement with the observation that endometriosis
occurs nine times frequently on the right hemidiaphragm than on
the left [4,6,14,15].
Coelomic Metaplasia
The second proposes the coelomic metaplasia mechanism that
causes endometriosis by metaplasia of mesothelial cells lining
the pleura and peritoneal surfaces into endometrial stroma and
gland [9,16,17]. Transformation of these cells may be affected
by physiological stimuli such as estrogen [18]. Support for this
hypothesis is observed in endometriosis patients with Mayer-
Rokitansky-Küster-Hauser syndrome who lack a functional
endometrium [19,20]. Rare cases of endometriosis can also occur
in men receiving high-dose estrogen. The coelomic metaplasia
hypothesis provides an explanation for pleural cases of thoracic
endometriosis. However, this fails to explain the right-sided
predominance seen in patients with thoracic endometriosis.
Prostaglandin
The third is a bioactive substance-mediated mechanism in
which high levels of prostaglandins, in particular prostaglandin
F2α. Prostaglandins are detectable in the plasma of women
during menstruation. Circulating prostaglandins increase with
menstruation [21,22-25] and causes vascular and bronchiolar
vasoconstriction, leading to the vasospasm and associated ischemia
within the lung [23,25,26]. This may result in alveolar rupture of
previously formed subpleural blebs and bullae, and subsequent air
leaks [23,25-27].
Hematogenous or Lymphatic Metastasis
An interesting hypothesis of metastasis suggests that
endometrial transplantation occurs through lymphatic or
hematogenous dissemination of endometrial cells, explaining
both the thoracic and other sites of implantation, in an analogous
manner to cancer metastasis [7,28,29]. Review of autopsy data
of humans with thoracic endometriosis shows that patients with
bronchopulmonary endometriosis usually have bilateral lesions,
whereas diaphragmatic and pleural diseases are predominantly
right sides [17]. Perhaps the most compelling evidence for the
benign metastasis hypothesis is derived from the investigations of
ectopic endometriosis lesions occurring in remote parts of the body
including the bone or brain [8,21,30-32].
Comment
Thoracic endometriosis is characterized by the presence of
endometrial-like glands and stroma within the lung parenchyma
or on the diaphragm and pleural surfaces. It remains unclear how
endometrial tissue migrates to the thoracic cavity, but it is often
associated with abdominal endometriosis. As none of the theories
proposed alone can account for all clinical manifestations of this
condition, so the etiology of thoracic endometriosis development
is likely multifactorial and closely intertwined with each other
hypothesis.
Disclosure Statement
The authors declare no conflict of interests regarding the
publication of this report.
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ISSN: 2574-1241
DOI: 10.26717/BJSTR.2021.40.006467
Atsushi Imai. Biomed J Sci & Tech Res