Results
A summary of clinical findings is shown in Table 1 . The 6 cases included 4 rhesus macaques and 2
cynomolgus macaques. The age of affected animals was 19.8 ± 6.0 years
(mean ± standard deviation). Affected macaques commonly presented with
anorexia with or without weight loss and abdominal pain. Only 3 of the 6
macaques had a history of progesterone treatment (medroxyprogesterone acetate,
Depo-Provera). Serosanguineous or sanguineous abdominal effusion was present in
3 of 6 macaques. One rhesus (case No. 6) was in heart failure at the time of
death and had serous abdominal effusion. Only 1 macaque (case No. 5) had a
history of heavy menses.
At necropsy, the uterus was commonly enlarged and disfigured or replaced
by dense connective tissue. Fibrous adhesions were commonly observed especially
between the omentum and the uterus, liver, spleen, and urinary bladder ( Fig. 1 ). In 3 cases, one or both ovaries were
not identified and were suspected to be incorporated or effaced by the fibrous
adhesions. Diffuse tan, red or black solid or cystic nodules were identified on
the uterus, urinary bladder, intestines and ovaries of 4 of the 6 macaques. The
gross lesions were similar in treated and untreated macaques ( Table 1 ).
Histopathological features of the exuberant decidualized endometriosis
tissue were very similar to lesions previously described in humans.
Endometriotic cysts and islands of decidualized stroma were separated by
variably dense bands of fibrous connective tissue ( Fig. 2 ). Hemosiderin-laden macrophages were often identified near
cysts ( Fig. 3 ). Cysts were lined by
pseudostratified, ciliated columnar epithelium and filled with erythrocytes,
cellular debris, and degenerate neutrophils and macrophages ( Fig. 4 ). Decidualized endometriotic stromal
cells were polygonal with distinct cell borders, abundant pale eosinophilic
cytoplasm and brightly eosinophilic, intracytoplasmic globules, which
occasionally marginalized the nucleus. Nuclei were round to oval with finely
stippled chromatin and 1 to 2 nucleoli ( Fig.
5 ). No mitoses were noted in any of the cases but anisocytosis and
anisokaryosis were present.
Endometrial granular leukocytes, a specialized type of gamma/delta T
cell, were scattered in the decidualized endometriosis stroma. These were small
cells with a high nuclear to cytoplasmic ratio ( Fig. 5 , small arrows). They contained eosinophilic granules
eccentrically clustered within scanty cytoplasm. The nuclei were dense and
deeply basophilic without recognizable nucleoli.
Decidualized stroma in these cases consistently stained positive for
nuclear progesterone and estrogen receptors, C10 and cytoplasmic vimentin ( Table 2 )( Figs. 6–9 ). Desmin, calretinin, cytokeratin, chorionic
gonadotropin, cytokeratin AE1/AE3, U22 HPL, and kermix P8 were inconsistent or
negative.
Discussion
Decidualization of the endometrium or ovarian tissue is a normal
physiological process and occurs in up to 100% of human pregnancies.
However, exuberant decidualized tissue, especially when it occurs in combination
with endometriosis, may endanger the mother and/or the fetus by causing pregnancy
complications or being mistaken for neoplasia. 1 , 18 , 20 Stroma of endometriosis lesions and endometrium
with hormonal stimulation from high progesterone may transform into decidualized
cells. The typical microscopic appearance of the transformed endometrial stroma
within the myometrium (internal), peritoneum, thoracic cavity, or skin (external) is
seen as islands of large polygonal cells with abundant eosinophilic cytoplasm
frequently containing intracytoplasmic droplets. These droplets have been described
as sulfated mucin and glycogen. 12 , 17 Decidualized stroma cells have
oval, centrally located nuclei with distinct magenta nucleoli and finely stippled
chromatin. While no mitoses are typically observed, there is often pronounced
anisocytosis and anisokaryosis. The population of transformed cells is often
embedded in swaths of histopathologically typical endometriosis: endometrial stroma,
endometrial glands lined by ciliated epithelium, pools of hemorrhage and
hemosiderosis. Furthermore there is often abundant lymphoplasmacytic inflammation,
hemorrhage and varying degrees of necrosis. 26
The cellular and nuclear atypia as well as the implantation of these cells
into the serosa of a myriad of abdominal organs may resemble a malignant neoplastic
process such as deciduoid mesothelioma, squamous cell carcinoma, mucin-producing
adenocarcinoma or carcinomatosis. 8 , 17 , 27 , 35 Gross
differential diagnoses for a decidualized stroma within the abdomen include
decidualized mesothelioma, endometriosis with granulomatous inflammation,
fibroplasia, granulation tissue and carcinomatosis, especially if tissue invades and
destroys the structural integrity of abdominal organs. 27 Atypical extra-placental trophoblastic
implantation of the peritoneal cavity is another differential in animals with a
history of pregnancy. 6 , 10 , 31 The rhesus macaques in cases Nos. 1 and 2 ( Table 1 ) were both exposed to a nitrosamine
carcinogen. Genital papillary mesotheliomas have been described in male rats given
nitrosamines. 15 Finally,
differential diagnoses for abdominal neoplasms following aromatase inhibitor
treatment, as in case 3, should include atypical mesenchymal proliferation induced
by the aromatase inhibitor treatment or potentially a neoplastic mesenchymal
transformation as is noted in cases of retroviral induced retroperitoneal
fibromatosis. 13 Retroperitoneal fibromatosis is histologically
distinct from deciduosis since it is composed of dense connective tissue without the
large, polygonal decidualized stromal cells. 28
In nonhuman primates, decidualization of endometriosis tissue occurs most
often under the influence of exogenous progestins or during pregnancy. 5 , 25 , 34 Here only 3 of
the 6 cases had received exogenous progestins (medroxyprogesterone acetate). None of
these animals were pregnant so we anticipate the endometriotic tissue decidualized
under the influence of elevated endogenous progesterone.
Recognizing the histopathological appearance of the decidualized cells and
correlating their presence with endometriosis are important criteria towards
appropriate diagnosis. Furthermore, immunohistochemical markers aid in confirming
the transformed endometrial stroma. We found the decidualized stroma stained
positive for nuclear progesterone and estrogen receptors, and cytoplasmic vimentin
as well as CD10 ( Table 2 ). These
histopathological characteristics were consistent with reported results in studies
of affected humans and nonhuman primates. Typical endometrial stroma stains
positively for common acute lymphoblastic leukemia antigen, or CD10, which is
expressed by hematopoietic neoplasms as well as the endometrium. 2 , 4 , 5 , 32 Additionally, the nuclei of the stroma have
positive staining for progesterone receptor and estrogen receptor. HCG and U22 HPL
staining are often assessed to rule out a trophoblastic implantation while
cytokeratin markers are evaluated to reject carcinomas as possible
diagnoses. 6 , 31 Scattered immunopositivity to both HCG and U22 HPL
observed in 2 of the 5 cases stained may represent a variation in
laboratory-specific sensitivity. Both positive cases were processed within the same
immunohistochemistry laboratory. Desmin has been reported to have variable staining
in decidualized endometriosis in humans, interpreted as metaplastic transformation
of the stroma into myofibroblasts or leiomyocytes, reinforcing the argument of
endometrial stroma plasticity. 7 In
all of our cases, the stromal cells were negative to desmin. A recent report of
pleural endometriosis in a rhesus macaque found that the endometrial stroma was
positive to calretinin, which is an immunohistochemical marker noted to demonstrate
strong nuclear and cytoplasmic staining of the normal endometrial stroma, while
showing decreased or negative reactivity in pathological uterine tissues to include
deciduosis, a finding which was supported in the immunohistochemical evaluation of
all 4 of the cases evaluated with calretinin. 3 , 4
In summary, endometrial stromal decidualization was confirmed based on the
histopathological features and immunohistochemical analyses of each case.
Macroscopically, the extensive, invasive spread of the endometriosis, multifocal
islands of decidualized stromal cells, abundant hemorrhage and variable, regional
necrosis mimicked malignancy. Histopathological atypia noted within the decidualized
cells represents a further confounding feature. These observations aid in
identifying and diagnosing such lesions in primates to serve as models for
decidualized endometriosis lesions in humans. Understanding endometrial
decidualization in nonhuman primates with endometriosis will aid to elucidate the
etiology of decidualized endometriotic stroma in women and further the investigation
of deciduosis diagnosis and treatment.
Materials|Methods
Six intact female macaques aged between 14 and 31 years (mean age, 19.8
years) were identified during clinical evaluations at the Armed Forces Radiobiology
Research Institute (AFRRI) or at the Wake Forest Primate Center at the Wake Forest
School of Medicine (WFSM). Macaque care and experimentation was approved by each
institution’s Institutional Animal Care and Use Committee and maintained in
accordance to federal and state laws including the National Academy of
Sciences’ Guide for the Care and Use of Laboratory Animals. 24 In addition, WFSM and AFRRI are
accredited by the Association for Assessment and Accreditation of Laboratory Animal
Care International. Two rhesus macaques were part of a chronic gastric
carcinogenesis study being conducted at AFRRI, were receiving nitrosating carcinogen
ethyl-nitro-nitrosoguanidine and were experimentally infected with
Helicobacter pylori . A third rhesus was part of an opioid and
pain receptors study at WFSM. The remaining rhesus macaque and the cynomologus
macaques were either on holding protocols or part of a WFSM breeding colony. Of the
6 cases, 3 had been treated with progesterone analogs (case Nos. 1, 3 and 6,
medroxyprogesterone acetate) and 1 with an aromatase inhibitor (case No. 4;
letrozole) for endometriosis.
After the initial clinical workup, cases were presented to pathologists at
the Division of Comparative Pathology at AFRRI or the Department of Pathology at the
Wake Forest University School of Medicine for pathologic evaluation. Diagnostic
necropsies were performed on each animal and tissues were collected. Affected
tissues, to include grossly recognized decidua were stained with hematoxylin
& eosin (HE) and various combinations of vimentin (Vector Laboratories,
clone SP20, rabbit monoclonal, 1:40), common acute lymphoblastic leukemia antigen
(CALLA, CD10, abcam®, clone 56C6, mouse monoclonal, 1:20), progesterone
receptor (Novocastra, Vision Biosystems, clone 1A6, mouse monoclonal, 1:100),
estrogen receptor alpha (Leica Microsystems, clone 6F11, mouse monoclonal, 1:100),
desmin (Epitomics, clone Y66, rabbit monoclonal, 1:250), cytokeratin AE1/AE3
(BioCare Medical, clone LU-5, mouse monoclonal, 1:50), kermix P8, human chorionic
gonadotropin (HCG, BioCare Medical, rabbit monoclonal, 1:200), human placental
lactogen (U22 HPL, Novocastra, Vision Biosystems, rabbit monoclonal, 1:200), and
calretinin. Secondary antibodies for the appropriate species were used at a 1:20
dilution (Super Sensitive™ Kit, BioGenex). Vector® Red (Vector
Laboratories, Burlingame, CA) or 3,3’-Diaminobenzidine (DAB) were used as
chromogens and slides were counterstained with Mayer’s hematoxylin. Negative
controls included slides treated with only secondary antibody. All
immunohistochemical stains were validated and performed by histology cores at each
location. Board certified veterinary pathologists or a board certified medical
pathologist evaluated all cases and slides.
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