Abstract
Background: A pulmonary endometriosis is one of the relatively rare forms of the extragenital endometriosis and in accordance to its clinico-pathological symptoms
is considered within the terms of the “thoracic endometriosis syndrome”, i.e. when functioning endometrium is found in the pleura, diaphragm, viae respiratoriae or
the pulmonary parenchyma itself.
Objectives
42 cases of this disease were observed. The patients age ranged from 16 to 61 years, thus the average being 40.5 ± 0.4 years.
Results
In the majority of cases the endometriosis affected the diaphragm and was accompanied by a pneumothorax with the corresponding symptoms complex,
while pulmonary foci occurred rarer, being asymptomatic or feigning some surgical and other pathology. The surgery and the histological study were crucial in
verifying the diagnosis. Progesterone and estrogen receptors, and Ki-67 production were detected immuno-histochemically in the endometrioid tissue of the lung foci.
Conclusion
The use of the comprehensive histological and immuno-histochemical methods was required to make the final diagnosis of the pulmonary endometriosis
more reliable. It has a great practical significance being one of the most important pre-requisites for prescription of an adequate treatment.
Correspondence to: Boris M. Ariel Saint-Petersburg Federal Research Institute
of Phthisiopulmonology, Healthcare Ministry of Russian Federation; Ligovsky
prospekt 2/4 193036 Saint-Petersburg Russia, Tel: (812) 534-3791; E-mail:
[email protected]
Key words: thoracic endometriosis syndrome, extragenital endometriosis,
pulmonary endometriosis, diaphragm lesion, pneumothorax, histological
verification of diagnosis
Received: November 28, 2017; Accepted: December 18, 2017; Published:
December 22, 2017
Introduction
Endometriosis is a growth of the tissue similar to the endometrium
outside the uterine cavity which is accompanied by a chronic
inflammatory reaction, leading in most cases to the development of
a pain syndrome and/or infertility. Currently, it is one of the most
common gynecological diseases. This pathology occurs in 2-10%
of women of reproductive age and almost in 50% of women with
infertility [1,2].
One of the relatively rare forms of the endometriosis is characterized
by the development of the endometrial tissue outside the reproductive
system. Extragenital foci may exist independently both as separate
formations and as components of the concomitant lesions [3,4]. The
cases of the extragenital endometriosis make 6-8% of the total number
of the endometriosis observed. Among the organs unrelated to the
reproductive system, there are the intestines, the urinary tract, and the
lungs that are most frequently affected [5].
Hart was the first to diagnose the pulmonary endometriosis (PE)
posthumously in 1912. He observed in a woman, aged 72, numerous
subpleural nodes varying from the size of a pea to that of a walnut. The
histological examination showed adenomyosis of the uterine origin; a
tumor in the patient’s uterus having been removed 22 years prior to
that [6].
Over the last decade the number of publications on the
endometriosis has markedly increased. The concept of the “thoracic
endometriosis syndrome” (TES) has been developed and used in cases
when the functioning endometrium is found in the pleura, the diaphragm,
the viae respiratoriae or the pulmonary parenchyma itself [7,8].
Channabasavaiah and Joseph [9] have presented results of an
analysis of 110 clinical cases of the histologically verified intrathoracic
endometriosis that were published between 2001 and 2007. Legras et
al. [10] have studied retrospectively 229 cases of the pneumothorax in
women described in the specialist literature written in English from
2000 to 2011 and state that the TES being diagnosed in 54 cases (24
per cent).
The question of how a functioning endometrium gets into the chest
remains as yet open [6, 11,12]. Sampson [13] was the first to suggest
that the endometrium is transferred from the uterine cavity into the
abdominal one through the fallopian tubes by way of the so-called
“retrograde menstruation”, that is, the discharge of some amount of
Dvorakovskaya IV (2017) Pulmonary endometriosis: Clinico-pathological approach to diagnostics and treatment
Volume 2(1): 2-5
Lung Breath J, 2017 doi: 10.15761/LBJ.1000119
blood into the pelvic cavity during menstruation. This kind of reflux
occurs in a large number of healthy women [14]. Sampson [13] also
hypothesized an existence of the metastatic, or embolic endometriosis,
which allows one to speculate about hematogenous routes of the
endometriosis propagation. Hobbs and Bortnick [11] confirmed this
hypothesis experimentally introducing the endometrium suspension
into the ear veins of rabbits, which resulted in the development of the
PE in 79 per cent of cases.
The TES manifests itself most often in the recurrent pneumothorax,
haemoptysis, cough or chest pain, and more rarely in the haemothorax
associated with the menstrual [2, 7, 15-17]. The PE is one of the rarest
forms of the TES. The most important clinical manifestations of the
former are cough, haemoptysis, and a feeling of heaviness in the chest
(a «heavy fur coat» symptom) that occur during menses, but not
necessarily in every menstrual cycle.
According to the literature, pneumothorax associated with the TES
is found in approximately 10-24 per cent of women with a spontaneous
pneumothorax [7, 16].
X-rays chest examination (mainly HRCT) reveals four variants
of the pathology: linear, or reticular opacities, small nodules, cystic
airspaces, thickened alveolar septa. These radiological findings,
particularly those combined with a haemoptysis and chest pain are
often regarded as an evidence of a tuberculous or a neoplastic nature of
the pulmonary lesion.
A diaphragm lesion is usually detected by accident during a surgical
intervention due to pneumothorax. Prior to the surgery this pathology
is very seldom detected because of a limited extent of the lesions and
low resolution of radiological methods.
Almost without exception, the disease affects a tendinous centre
of the right diaphragm dome and may appear in two kinds. The first
one takes the form of blue or purple endometrious implants under the
parietal pleura up to 5 mm in size. The second are round or slit-like
defects in the diaphragm.
The lack of specific symptoms, of laboratory markers, and
characteristic radiological patterns makes the preoperative diagnosis
of PE difficult. It is often finally diagnosed only after a confirmation
by the histological methods, among them the immuno-histochemistry,
including estrogen and progesterone receptors expression [15].
Therefore, the surgical intervention is often necessary on
diagnostic and therapeutic purposes. Though the operation does verify
the diagnosis as a rule and removes any heterotopic endometrium
lesions, this kind of treatment remains incomplete [7, 17] without
a suppressive hormonal therapy. It aims at an ovulation blocking, a
suppression of the estrogen secretion and epithelial growth supression
in the endometrious focus [18].
A relatively small number of the TES cases described in the world
specialist literature and the lack of its pathognomonic clinical picture
prompted us to summarize our own experience in the diagnostics and
treatment of this disease.
Methods
We’ve analyzed 42 cases of the TES observed in our hospitals over
the period from 2004 to 2016. The patients age ranged from 16 to 61
years, thus the average being 40.5±0.4 years.
35 patients were hospitalized due to a spontaneous pneumothorax,
3 with rounded tumorous masses, 1 with a cyst, and 3 with an infiltration
in the lung tissue. Significantly, in 41 patients the pathological process
was localized in the right lung.
Results
The main complaints of all hospitalized patients are listed in the
Table 1.
In most cases, there was a chest pain (85.7 per cent); haemoptysis
was found less often (9.5 per cent). Dyspnea was noted only in 31
patients with pneumothorax; 6 women suffered from infertility. In
the anamnesis, 5 patients had uterine myoma, and there was ovary
endometrial cyst in 2 patients.
HRCT of the chest detected rounded shadows in the lungs (3
cases), infiltrates with thin-walled cavities (6 cases), lung cyst (1 case),
bullae of various diameter (6 cases), and a mass in the paravertebral
region considered as a neurinoma (1 case) (Figure 1). In the same time
no changes in the lung tissue were detected in 26 of 42 cases (61.9 per
cent of the patients).
Unfortunately, a preoperational examination doesn’t allow us to
suggest the TES in any case, as CA-125 expression doesn’t indicate
the possibility of it either. At the same time, a retrospective analysis of
the post-operative data suggested that an essential prerequisite to this
diagnosis did exist.
Pre-operational diagnoses were the following: primary spontaneous
pneumothorax in 35 cases, infiltrative pulmonary tuberculosis in 3
cases, lung haemosiderosis, neurinoma of mediastinum, lung tumour,
and lung cyst - each being in one.
The surgical intervention was performed in 37 of 42 patients. Of
those 35 women with pneumothorax, 30 (85.7 per cent) were operated.
Atypical lung resection was performed in 27 cases (90 per cent of
the patients), costal pleurectomy in 28 cases (93.3 per cent) and the
resection of the diaphragm tendon centre in 25 cases (83.3 per cent).
Of 7 patients without pneumothorax 6 were subjected to the
atypical lung resection and 1 to the lobectomy.
In all cases а histological examination of the surgical material
was performed. Paraffin sections were stained with haematoxylin
and eosin, alcian blue, and picrofuchsin by van Gieson. Immuno-
histochemistry was performed using antibodies to progesterone and
estrogen receptors as well as mouse monoclonal antibodies to Ki-67
and bcl 2 (Dako, Denmark).
In correlating clinical and histological data, the TES was diagnosed
in all cases and may be subdivided into following categories: perforation
of the right dome of the diaphragm with histologically identfied
endometrial implants (6 patients); intrapulmonary endometrial
heterotopias in the form of nodes, infiltrates and cysts (11 patients);
multifocal lung and diaphragm lesions (1 patient). A perforation of the
diaphragm right dome without histologically identified endometrium
(“porous diaphragm”) was observed in 24 cases.
Complaints Patients (n=42)
abs. number per cent
Chest pain 36 85,7
Dyspnea 31 73,8
Dry cough 21 50,0
Infertility 6 14,3
Haemoptysis 4 9,5
Table 1. Complaints of patients with the thoracic endometriosis syndrome.
Dvorakovskaya IV (2017) Pulmonary endometriosis: Clinico-pathological approach to diagnostics and treatment
Volume 2(1): 3-5
Lung Breath J, 2017 doi: 10.15761/LBJ.1000119
The macroscopic assessment of removed lungs detected cysts
with dark brown material (6 cases). The walls of the cysts were thick,
their inner surface smooth (5 cases), or with papillary outgrowths (1
case). 5 remaining observations revealed small hemorrhage foci in the
subpleural areas.
The microscopic examination detected numerous clusters of
endometrial glands with a cytogenic stroma. The structure of these
glands corresponded to various phases of the menstrual cycle 9 (viz.
a proliferation or secretion stage) presented in different quantities.
The endometrial type of epithelium of the glands was usually
pseudostratified, flattened or columnar; cell nuclei were located at the
different levels; the cytoplasm contained secret drops; here and there
some signs of epithelium desquamation were noted. In the alveolar
lumina and the lung interstitium hemosiderin deposits were often
found. The glandular stroma was represented by elongated cells with
spindle-shaped nuclei, in some places with decidualization features
(Figure 2). In 5 cases a cystic transformation of glands was observed
along with haemorrhages around them. Some haemosiderin deposits
and a fibroblastic transformation of a cytogenic stroma were evident
in the most cases.
In all cases the immuno-histochemical study was performed. It
revealed the progesterone and estrogen receptors expression in the
gland epithelium and cytogenic stroma cells (Figure 3 A, B) as well as
expression of the oncoprotein bcl-2 in the gland epithelium and moderate
proliferative activity (Ki-67) in the cytogenic stroma (Figure 3 C).
Shown below are two examples from our observations.
Example 1. Patient F., 52 years old. The clinical diagnosis was a
tumor of the right lung lower lobe. Six years before, extirpation of
the uterus without appendages was performed on the account of the
uterus myoma with adenomyosis; the patient suffered from infertility.
6 years after the surgery there were complaints about periodic aching
pains in the chest, cough and haemoptysis. The radiography of the
thorax revealed a round shadow of 4 cm in diameter in the lower
lobe of the right lung. HRCT showed a rounded formation, 4х3х2,5
cm in size, heterogeneously structured with well-defined contours.
The examination failed to verify the precise diagnosis, so the right
lower lobectomy was performed. Macroscopically, a “honeycomb”
type formation with well-defined contours and small cavities up
to 0.7 cm filled with thick brown liquid was detected. There was a
dense homogeneous fibrous tissue between cavities. The histological
examination revealed cystic transformed endometrioid glands with a
proliferating epithelium on their walls as well as a papillae formation
and a fibrous cytogenic stroma, along with a leiomyomatous hyperplasia
around glandular structures (Figure 4).
Example 2: Patient A., 42 years old. Clinical diagnosis was the right-
side spontaneous pneumothorax. On the first day of the menstrual
cycle pain in the right half of the chest appeared. It was accompanied
by a dry cough and a slight dyspnea. Chest radiography revealed a
right-side pneumothorax with a 50 per cent atelectasis and a shift of
the mediastinum to the left. Upon admission to the hospital a right-side
diagnostic thoracoscopy was performed with a drainage of the pleural
cavity. The tendon center of the diaphragm showed perforations
and endometrial implants (Figure 5). HRCT of the chest revealed no
changes in the lung tissue. The right-side videothoracoscopy, resection
of the diaphragm tendon center and subtotal costal pleurectomy were
performed. Macroscopically, some perforations in the tendon centre
and brownish nodules with well-defined contours up to 0.5 cm were
detected. They were located on the pleural diaphragm surface without
penetrating through it. The histological examination showed some
cystic endometriod lesions on the fibrous background.
In this case, as well as in all others, the onset and the disappearance
of clinical and radiological symptoms coincided with the beginning
and the end of the menstrual cycle. Nevertheless, this fact escaped the
physisians.
Discussion
As a clear proof of the words once uttered by the well-known Russian
oncomorphologist Golovin [19,20], the extragenital endometriosis
confirms that every tissue is a historically formed stable unity possessing
certain properties and morphogenetic potencies, which do not
disappear completely even in case of abnormal interrelations between
an organism and a tumor. This approach is extremely important for
understanding the PE as a pathological process toto coelo.
In most of our observations, the endometriosis affected the
diaphragm and was accompanied by the pneumothorax with a
corresponding symptoms complex, while the pulmonary heterotopia
Figure 1. HRCT chest scans of patients with pulmonary endometriosis A – lung tissue infiltration; B –small cavities; C – peripheral nodules.
Figure 2. Pulmonary endometriosis. A - islets of endometrial glands proliferation. In the
alveolar lumina there are hemosiderin deposits. Haematoxylin and eosin staining (X 100);
B - proliferating epithelium of the glands with secret drops in cytoplasm. Stroma with
decidualization features. Haematoxylin and eosin staining (X 160).
Dvorakovskaya IV (2017) Pulmonary endometriosis: Clinico-pathological approach to diagnostics and treatment
Volume 2(1): 4-5
Lung Breath J, 2017 doi: 10.15761/LBJ.1000119
occurred rarer being asymptomatic or feigning certain surgical and
other pathology.
It is worth mentioning that the lesion of the left half of the chest
was diagnosed only in one case (viz. implants in the left dome of the
diaphragm and the left lung), which confirms the fact that TES is the
right-sided pathology. We suggest that the reason of this selectivity is
the fact that the right dome of the diaphragm together with the liver,
although not rigidly bound, works during the breathing like a piston
providing a “suction effect”. Supposedly, this is also the reason why it is
exactly the space under the right diaphragm dome where certain amount
of the menstrual blood can get from the pelvis. The blood resorption
is carried out with the active participation of the lymphatic apparatus
of the peritoneum [21]. Endometrial fragments reach the subpleural
space through the lymphatic vessels perforating the diaphragm and
remain fixed there in most cases. The subsequent necrosis and lysis of
the endometrium may lead to the perforation defects. Hypothetically it is
possible that in rare cases small endometrium fragments reach the superior
vena cava through the mediastinum lymphatic vessels and then penetrate
into the pulmonary parenchyma forming nodes, or cysts.
The clinical and morphological hypodiagnostics of the TES is
conditioned not only by its rarity, but by the lack of the comprehensive
complex analysis and correlation of the anamnestic, clinical, and
histological data as well.
Given the increasing incidence of the endometriosis, the
pulmonary one among others, it seems essential to include this disease
into the differential diagnostics range, particularly where women of
childbearing age with the unclear right-sided pulmonary pathology
and compromised gynecological history are involved. In such cases, it
is advisable to recruit gynecologists so as to exclude the adenomyosis
and the pelvic endometriosis. In the case of the obscure recurrent
pulmonary diseases it is imperative to carry out the MRI of the small
pelvis organs.
Our data allow to determine some important and reliable features
of the TES as follows: the predominantly right-side localization
of the disease, the relatively young age of the patients, the cyclic
recurrence of the haemoptysis and discomfort or pain in the chest, the
recurrent right-side pneumothorax, the correlation of the onset and/
or regression of the radiological symptoms with the beginning and/or
end of the menstrual cycle, one or the other of gynecological problems
(viz. infertility, pelvic pain, algomenorrhea), and surgeries on the pelvic
organs in the anamnesis.
The diagnostic surgery requires an extensive use of the whole
operation material with cutting out samples for the histological
examination of all affected lung areas, since the endometriosis
microscopic features in different, even neighbouring parts of the lung
may vary considerably. From the diagnostic standpoint, the essential
morphological distinctive feature of the PE is a combination of the
stability, progression or regression signs within the same or in the
adjacent samples of the lung tissue. To make the final diagnosis of
the TES more reliable, the use of the comprehensive histological and
immuno-histochemical methods is required. The precise diagnosis
of the endometriosis is of great practical importance because it is a
prerequisite for a selection of the adequate treatment.
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Figure 3. Pulmonary endometriosis: A – expression to progesterone receptors in glandular epithelial cells (X200); B – identical with estrogen receptors (X200); C – Ki-67 expression in the
cytogenic stroma (X100).
Figure 4. Pulmonary endometriosis with papillary structures and leiomyomatous
hyperplasia. Van Gieson staining (X 160).
Figure 5. Diaphragm lesions revealed in operation. A – perforations in the diaphragm
tendon center; B – endometrioid implants.
Dvorakovskaya IV (2017) Pulmonary endometriosis: Clinico-pathological approach to diagnostics and treatment
Volume 2(1): 5-5
Lung Breath J, 2017 doi: 10.15761/LBJ.1000119
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