Uterine adenomyotic cyst with markedly elevated serum CA19‑9 and CA125 levels: A case report

Uterine cystic adenomyosis is an uncommon gynecological disease ( 1 ). Its characteristic features include ectopic endometrial glands, stromal invasion of the myometrium, cystic part of old blood, with diffuse or focal widening of the junctional zone and bright foci or linear striations in the myometrium on T2-weighted magnetic resonance imaging (MRI) scans. Buerger and Petzing ( 2 ) pointed out that, although uterine adenomyosis may have a cystic part of old blood, the scope of the area is small, generally not >5 mm, and large cystic lesions are rare, which are called adenomyoma bone cyst (adenomyotic cyst), bursa sex gland fibroids (cystic adenomyoma) or bursa sex steroid myopathy (cystic adenomyosis). Large adenomyotic cysts (≥1 cm in diameter) are uncommon; to date, only ~70 cases of this type of lesion have been reported worldwide according to a literature search performed in MEDLINE and the Foreign Medical Literature Retrievals Service database using search term ‘adenomyotic cyst’ from 1992 to 2022. The serum concentration of cancer antigen 125 (CA125) has been revealed to increase during endometriosis and measurement of the serum CA125 concentration is widely used as a supplementary test for diagnosing the disease and evaluating therapeutic effects ( 3 ). Another cancer antigen, CA19-9, has recently been reported to increase endometriosis, but it rarely increases above 1,000 U/ml ( 4 ). However, the literature has reported only seven cases of adenomyotic cyst with elevated CA19-9 or CA125 levels ( Table I ). The present report presents a case of a uterine adenomyotic cyst with markedly elevated serum CA19-9 and CA125 levels.

CA19-9, first reported by Koprowski et al ( 6 ), is mainly found in the fetal stomach, intestinal epithelial cells and pancreas, and as a carbohydrate antigen recognized by a monoclonal antibody in a human colon cancer cell line. In addition to being a highly sensitive tumor marker for pancreatic and bile duct cancers, it has been reported to be highly sensitive for gynecologic tumors, such as endometrial carcinoma or ovarian cancer. Recently, CA19-9 was also reported to be increased in patients with endometriosis and adenomyosis ( 7 ), but it rarely exceeds 1,000 U/ml, as it did in the present case. Increased serum CA125 levels have also been proposed as a diagnostic tool for cystic adenomyosis. Cucinella et al ( 5 ) and Zhao et al ( 8 ) respectively described a large adenomyotic cyst with slightly elevated CA125. Furthermore, two cases of giant adenomyotic cyst originating from the cervix with raised CA125 levels were also reported by Pontrelli et al ( 9 ) and Isik et al ( 4 ). Certain studies reported that preoperative CA125 levels as high as 1,212.00 U/ml returned to normal after excision of these areas ( 10 , 11 ). Serum CA125 levels are generally elevated in patients with giant adenomyotic cyst. A large-magnitude increase in the serum levels of both CA125 and CA19-9 in patients with cystic adenomyosis is rare ( 12 , 13 ). In the present case, serum CA125 was 642 U/ml and CA19-9 was as high as >1,000 U/ml prior to surgery, which decreased after tumor removal, consistent with previous reports. The present study expands the knowledge on cases with significantly increased CA19-9. However, it was not possible to determine the reason for the abnormally high serum level of CA19-9. Similarly, MRI and other imaging studies ( 14 , 15 ) suggest that hemorrhage in uterine adenomyosis lesions in the present case may damage the ovaries, uterus and nearby tissues, causing surrounding tissue adhesion, damaging the peritoneal barrier and possibly causing CA19-9 leakage into the circulation. In benign biliary tract diseases such as acute cholangitis, the bile duct epithelium is reported to be damaged by inflammation and biliary CA19-9 and CA125 may leak into the circulation ( 3 ). The differential diagnosis (such as biliary tract diseases, ovarian disease and enteropatia), was excluded by ultrasonic examination, MRI findings, CT scan, hysteroscopy check and pathological results. MRI imaging and 3D ultrasound have recently been clinically applied in the gynecologic field, with reports that may be useful for the diagnosis of adenomyosis ( 16 ). MRI may now detect the normal junctional zone and adenomyotic cysts ( 17 ). The Myometrial location (intramural, submucous, subserous), Uterine site (midline, paramedian, lateral); Structure (cystic, mixed, polypoid), Contents (clear, hemorrhagic), Level (fundus, body, cervix) and Endometrial or inner lining (endometrium, metaplastic) (MUSCLE) classification was suggested for evaluating cystic adenomyosis ( 18 ). The patient of the present study may be classified as an intramural cystadenoma, namely M1 U1 S1 C2 L2 E2. MRI is considered clinically valuable in this respect. To distinguish the condition from other types of intramural cyst, histological diagnosis is necessary to identify the endometrial inner layering and the presence of outer myometrium. To prevent malignant tumor spread, a laparotomy operation was performed. There is doubt regarding the nature of such rare voluminous cysts in young females prior to surgery, considering patient age at symptom occurrence ( 8 ). The postoperative decrease of CA19-9 was slower than that of CA125. It remains unclear whether this difference was caused by a difference in the half-life of these two tumor markers in the circulation. However, unlike CA125 in adenomyotic cyst, CA19-9 appears to not be a sensitive marker of adenomyotic cyst. In conclusion, larger adenomyotic cysts are rare, while small adenomyotic cysts of <5 mm in diameter have been detected in hysterectomy specimens. In addition, 70 cases of adenomyotic cyst have so far been reported in the literature. In the case of the present study, serum CA19-9 and CA125 levels were significantly increased, which has been rarely reported. Due to these laboratory test results, it was not possible to make a confident differentiation of benign vs. malignant tumors. The ultrasound results and MRI suggested a diagnosis of a mass of uterine origin. In addition, the operation and pathology examination confirmed cystic lesions. However, additional case reports are required to further elucidate the pathogenesis and clinical characteristics of this rare disorder.

A 32-year-old female [gravida 3 (referred for artificial abortion due to abnormal fetal development in 2019; one missed abortion in 2020), para 1 (gave birth to a live healthy full-term baby in 2011)] presented at the Northwest Women's and Children's Hospital (Xi'an, China). Ultrasonography was performed during the follow-up after the missed abortion, revealing an intrauterine cystic lesion without any symptoms of menorrhagia, chronic pelvic pain or dysmenorrhea. Following that, a hematologic examination and tumor marker detection were performed, which revealed CA125 levels of 175 U/ml and CA19-9 of >1,000 U/ml. Given the abnormally high tumor marker levels, abdominal CT scanning and gastroscopy were all completed but did not reveal any evidence of gastrointestinal malignant lesions. The patient suddenly experienced pelvic pain and was referred to the department for a thorough gynecological evaluation. Measurement of serum CA19-9 and CA125 levels. Blood samples were taken and serum was obtained according to standard protocols. CA125 (normal ranges: CA125, 0-35 U/ml; CA19-9, 0-27 U/ml) were measured using the electrochemiluminescence immunoassay on a Roche Cobas e 801 analyzer (Roche Diagnostics). Imaging . CT scanning parameters were 128x0.628 mm collimation with a reconstruction interval of 1 mm, rotation time of 0.75 sec, tube voltage of 120 kV and 200 mAsec (Brilliance iCT; Philips Healthcare). A Color Doppler Ultrasound (U22; Philips Healthcare) diagnostic instrument was adopted with 7.5 MHz endovaginal probe. MRI was performed with a 1.5-T superconductive magnet unit (Picker International Co. Ltd.). T1-weighted spin-echo images (T1-WI; repetition time, 600 msec; echo time, 20 msec) and T2 weighted spin-echo images (T2-WI; repetition time, 2,000 msec; echo time, 80 msec) were obtained. Immunohistochemistry . Tissue samples were fixed in a 10% (v/v) solution of buffered formalin for 24 h at 4˚C and then dehydrated, cleared in xylene and embedded in paraffin. Paraffin sections (5 mm) were mounted on silane-coated slides, de-waxed and rehydrated. For antigen retrieval, the sections were treated with 10 mM citrate buffer, pH 6.0 in a water bath (30 min at 95˚C), then treated with 1.5% (v/v) H 2 O 2 in methanol for 10 min for quenching the endogenous peroxidase activity and finally equilibrated in 10 mM PBS-0.05% v/v Tween 20 pH 7.5. Nonspecific binding was reduced by incubation in 1% BSA (Cytiva) for 60 min. Subsequently, the slides were incubated with rabbit polyclonal anti-CA125 (cat. no. HPA065600; dilution, 1:100; MilliporeSigma) or mouse monoclonal antibody anti-CA19-9 (cat. no. 399S; dilution, 1:100; MilliporeSigma) in a humidified chamber for 22 h at 4˚C. After washing in PBS-Tween 20, the sections were incubated with biotinylated goat anti-rabbit or horse anti-mouse immunoglobulin (cat. no. CY-4500 or CY-2500, respectively; 1:100 dilution; Vector Laboratories, Inc.; Maravai LifeSciences) for 30 min at 25˚C, and then treated with avidin-biotinylated peroxidase complex (Vector Laboratories, Inc.; Maravai LifeSciences) for 30 min at 28˚C. The bound antibodies were visualized with diaminobenzidine and H 2 O 2 in PBS, pH 7.5 according to the manufacturer's instructions (Vector Laboratories, Inc.; Maravai LifeSciences). Finally, the tissues were stained with Gill's hematoxylin, dehydrated and mounted with coverslips. Negative controls were prepared by substituting the primary antibodies with rabbit IgG (cat. no. 0023305; dilution, 1:20; Thermo Fisher Scientific, Inc.) or mouse IgG (cat. no. 12371; dilution, 1:20; EMD Millipore). History of menstruation. The patient had attained menarche at the age of 14 years. The patient had a history of a 28-day regular menstrual cycle without hypermenorrhea. Pelvic examination. The uterus was displaced to the right of the median line and was estimated to be larger than a goose egg. There were no pelvic tenderness or nodules. Pelvic examination revealed a normal vagina, vulva and adnexa and an enlarged retroflexed uterus. Hematologic examination. Laboratory tests revealed anemia (hemoglobin concentration, 102 g/l (normal range, 115-150 g/l). The biochemical profile was otherwise unremarkable. The serum concentration of CA125 and CA19-9 was elevated at 642 U/ml and >1,000 U/ml, respectively. Ultrasonic examination. Ultrasonography displayed a multi-locular cystic mass on the posterior wall of the uterus. Color power Doppler revealed a difference from a leiomyoma. The mass was diagnosed as uterine adenomyoma ( Fig. 1 ). The ultrasound of the hepatobiliary duct, pancreas and spleen exhibited no abnormalities. An abdominal CT scan indicated no abnormal density lesions in the liver, bile duct, pancreas, spleen or gastrointestinal tract. MRI findings. From the MRI findings ( Fig. 2 ), the abnormal signal shadow and central hemorrhagic cystic in the posterior compartment of the uterus were considered adenomyoma. The mass measured 53x48x41 mm and T2-WI displayed the cyst as an area of high intensity. The normal uterine cavity was visualized as a line near the cyst. It was slightly hyperintense on T1- and T2-WI, with an internal fluid level, typical for the layering of simple and hemorrhagic or proteinaceous fluids. Hysteroscopy check. Hysteroscopy visualized a normal uterine cavity and bilaterally patent tubal ostia ( Fig. 3 ). Intraoperative findings. Laparotomy surgery was performed. The surgery was very similar to that in the case report of Cucinella et al ( 5 ). Enlargement of the posterior wall of the uterus was seen and chocolate-colored fluid flowed out of the posterior wall after incision. No abnormality was found in the appearance of bilateral fallopian tubes and ovaries. The excised lesion was sent for pathological examination ( Fig. 3 ). Tissue distribution of CA19-9 and CA125. The resected specimens were fixed in 10% formalin, embedded in paraffin and examined by immunohistochemical staining with anti-CA125 and anti-CA19-9 to determine the tissue distribution of each tumor marker. CA19-9 and CA125 were not expressed in the adenomyotic cyst which results not shown. Changes in serum CA19-9 and CA125 le vels. Both tumor markers were assayed using commercially available radioimmunoassay kits (Centocorl) once per week. CA125 decreased below the cut-off level (0-35 U/ml) at ≥4 weeks after the operation, but CA19-9 did not decrease below the cut-off level (0-37 U/ml) until ≥6 weeks after the operation ( Fig. 4 ). The patient underwent GnRha therapy for six months and there was no evidence of recurrence throughout the follow-up.