Table of Contents Author Guidelines Submit a Manuscript
Case Reports in Obstetrics and Gynecology
Volume 2013 (2013), Article ID 238156, 5 pages
Case Report

Abscessed Uterine and Extrauterine Adenomyomas with Uterus-Like Features in a 56-Year-Old Woman

1TOBB ETU Hospital, Department of Pathology, Yasam cad. No:5 Sogutozu, 06510 Ankara, Turkey
2TOBB ETU Hospital, Department of Gynaecology, Ankara, Turkey

Received 14 May 2013; Accepted 1 July 2013

Academic Editors: P. McGovern and K. Takeuchi

Copyright © 2013 Asiye Safak Bulut and Tevfik Uğur Sipahi. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Adenomyosis, also known as endometriosis interna, is the presence of endometrial glands and stroma within the myometrium. Its localised form is called adenomyoma and mimics a leiomyoma. Rarely, adenomyomas are located outside the uterus and some of them form uterus-like masses with a thick muscle wall and an endometrium-lined central cavity. They are generally located in the ovary or broad ligament, and, although they are closely related to endometriosis, their pathogenetic mechanisms are different from each other. Müllerian duct fusion defect and subcoelomic mesenchyme transformation theory are two possible pathogenetic mechanisms for this rare entity. Here we report abscessed uterine and extrauterine adenomyomas forming uterus-like masses in the left and right broad ligament and an ectopic adrenal tissue in the left paraovarian region in a 56-year-old woman. Although there is a reported abscessed adenomyosis in the literature, this is the first abscessed extrauterine uterus-like masses with synchronous pelvic pathologies like endometriosis, leiomyomas, adenomyosis, an endometrial polyp, an endocervical polyp, and an ectopic adrenal tissue. This benign lesion gives the impression of leiomyoma, a uterine malformation, or even malignancy preoperatively. Frozen section helps in differential diagnosis.

1. Introduction

An adenomyoma is a circumscribed, nodular aggregate of smooth muscle, endometrial glands, and, usually, endometrial stroma within the myometrium [1]. The downgrowth and invagination of the basalis endometrium into the myometrium are the current developmental theory [2]. Although there are few reports describing abscess formation in endometriosis, there is only one reported case of abscessed adenomyosis [35]. Adenomyomas may be located within the myometrium, or it may involve or originate in the endometrium and grow as a polyp [1, 6]. Extrauterine adenomyomas located at the ovary, broad ligament, and uterosacral ligament are rare, and those mimicking a uterus are even rarer [711]. Here we report multiple abscessed adenomyomas forming uterus-like masses in the left and right broad ligament and in myometrium. There were also leiomyomas and adenomyosis in the myometrium, adhesions in the pelvis, and fluid in Douglas fossa. The diagnosis was made by frozen section. Postoperative period was uneventful.

2. Case Presentation

A 56-year-old multiparous (gravida 2, para 2) woman presented with menorrhagia after three months' amenorrhea and pelvic and lumbar pain. There was no history of a chronic disease, pelvic inflammatory disease, intrauterine device, or tubal pathology. On physical examination, she was found to have lobulated hard masses filling the pelvis up to the umbilicus. She had no fever. Transvaginal ultrasonography showed well-defined nodular masses around the uterus obscuring the discrimination between uterus and ovaries. Serum CA 19-9 and CA-125 levels were 32.94 U/mL and and 46.60 U/mL, respectively. In the whole blood, erythrocyte, leukocytes, and thrombocyte counts were /UL, /UL, and /UL, respectively. Hemoglobin was 9.8 g/dL; haematocrit was 28.5%. CRP was 249.1 mg/L. Urine culture was negative. Magnetic resonance imaging revealed a giant hypervascular lobulated mass measuring  cm, with central necrosis, filling the pelvis, indenting the uterus, rectosigmoid, and bladder. It was closely related to uterine corpus so it was thought to be originated from it (Figure 1). It was reported to be a large necrotic leiomyoma without an exclusion of malignancy. Laparotomy was planned in order to rule out a pelvic malignancy.

Figure 1: Lobulated mass, filling the pelvis and indenting uterus in MRI.

Intraoperative evaluation revealed four leiomyoma-like masses in the right broad ligament measuring 5 to 10 cm in diameters. There was a 6-cm-diametered one in the left broad ligament and two other ones measuring 7 cm and 5 cm in the posterior and right walls of the uterus. There were also intraperitoneal adhesions and 20 cc fluid in the Douglas fossa. One of the masses located in the right broad ligament was sent for frozen evaluation. It was a peritonealised surfaced nodular mass with  cm dimensions and had a  cm central cavity containing pus. The cut surface of the mass was somewhat like a uterus with a thick muscle wall and an endometrial cavity-like central space with some nodularity in the wall.

In microscopic examination, the cavity was lined by endometrial type glands and stroma and infiltrated by leukocytes, lymphocytes, plasmocytes, hemosiderin-laden macrophages, and hystiocytes (Figure 2). The inflammation was extending to the thick muscle wall. There were small endometriotic foci and small leiomyomas between the muscle bundles. There was no architectural complexity or cytologic atypia within the epithelium, and mitotic figures were infrequent. The smooth muscle component was arranged in irregular fascicles. There was no mitotic activity or necrosis. As the mass was reminiscent of a uterus macroscopically and microscopically, it was thought to be one of the corns of a bicornuate uterus. But it was learned that it was not connected to the uterine body, tube, or ovary. There were also other similar masses in the pelvis. So a diagnosis of abscessed adenomyoma was made with frozen section. Total abdominal hysterectomy and bilateral salpingo-oophorectomy with excision of intraligamentary masses and intraperitoneal adhesions were performed.

Figure 2: Inflamed endometrium-lined inner surface of uterus-like mass (HE, original magnification is 40).

In the hysterectomy specimen, there was a similar mass with 9.5 cm diameter in the right wall of the uterus. There were Nabothian cysts and a  mm polypoid lesion in the cervix and a  mm polyp in the endometrial cavity. Five leiomyomas up to 25 mm diameter and a few small bloody cysts were observed within the myometrium. The left wall of the uterus was yellowish in color. Ovaries contained small cysts, and there was a 4 mm orange colored nodule between the left ovary and left tuba.

The right-sided uterine mass and intraligamentary masses had a similar microscopic feature with the one evaluated by frozen section. There were endometriotic foci and leiomyomas, one of which is palisaded type, in the myometrium. Ovaries contained follicular cysts. The orange colored nodule was consistent with an ectopic adrenal tissue mostly formed of adrenal cortical cells (Figure 3).

Figure 3: Ectopic adrenal tissue (HE, original magnification is 40).

In the microbiological examination, no microorganisms were isolated from the foci of abscess in both aerobic and anaerobic cultures, and there was not another primary source of infection. So, the cause of inflammation remained unknown. The patient's postoperative period was uneventful.

3. Discussion

The presence of tumor-like masses formed of endometrial glands, specialized endometrial stroma, and smooth muscle in extrauterine localisations is rare, and the terminology is somewhat arbitrary for these lesions. The term “extrauterine adenomyoma” is preferred by most authors as they are similar in most respects to their more common uterine counterparts [7, 8, 12]. Some other authors used the term “uterus-like mass” as an alternative terminology [9, 10, 1315]. Adenomyomas that share some features of uterus-like masses are described as “adenomyoma with uterus-like features” by some authors [1618]. Matsuzaki et al. used the term “endomyometriozis” for a mass lesion in the uterosacral ligament [11]. Our case had the features of both adenomyoma and uterus-like masses and defined as “adenomyomas with uterus-like features”.

Although the first uterus-like mass is said to be described by Cozzutto in 1981, Cranstoun reported a cystic adenomyoma of uterus in 1922 [13, 19]. The mass he presented was very dark colored and adherent to the parietal peritoneum, omentum, and gut by its anterior surface. The rupture of the mass caused the escape of large quantities of brown muddy-looking fluid. Uterus was irregularly enlarged and contained three fibromyoma-like masses. Each mass was composed of uterine tissue containing many spaces filled with degenerated blood-clot and communicated with the others. The large cyst was continuous with the edge of the largest fibromyoma-like mass that was located at the upper left corner of the uterus. The cystic mass was also composed of uterine tissue with many spaces filled with degenerated blood-clot in the wall. Left and right ovaries and tubas were macroscopically normal. The explanation of the mass was the degeneration and distention that started centrally and expended to the upper part of the tumor that least resistance was encountered on the abdominal site. Although the diagnosis was a cystic adenomyoma of the uterus, their uterine tissue composition and the presence of endometrium-like cavity and blood-clot in the center were so reminiscent of uterus-like masses later defined.

Carinelli et al. stated that there are only 19 extrauterine adenomyomas in the English-language scientific literature [18]. These uterus-like masses can be located in various extrauterine sides including the broad ligament, ovary, and uterosacral ligament [11, 14, 16, 17]. They typically exhibit an organoid arrangement consisting of a single central cavity lined by endometrial type mucosa with surrounding myometrial like tissue. Our case had such an organoid arrangement with small endometriotic foci and leiomyoma-like arrangements in the smooth muscle component. The uterine and extrauterine adenomyomas were abscessed in our case. Although abscess formation is reported in the endometriomas [3, 4], only Erguvan et al. reported an abscessed adenomyosis [5]. In Martino et al.'s case the abscess occurred iatrogenically following fine needle aspiration [3]. Lipscomb et al. hypothesized that the abscess in their case might have developed following haematogenous spread of bacteria from an urinary tract infection because the same organism was recovered from the patient's urine and the abscess cavity [4]. In Erguvan et al.'s case, no microorganisms were isolated from the foci of abscess in both aerobic and anaerobic cultures, and the cause of infection remained unknown as in our case.

A Müllerian duct fusion defect is the possible mechanism for the pathogenesis of uterus-like masses. This theory is based on a developmental abnormality occurring during the formation of the female genital tract. Lack of fusion of the Müllerian ducts in a localized area, or throughout the length of the ducts, may explain various duplications or atresias of the uterus [20]. In our case, the patient has a normal uterus, cervix, fallopian tubes, and ovaries. She had no renal abnormality.

Another theory is the subcoelomic mesenchyme transformation theory [9, 18]. The subcoelomic mesenchyme or secondary Müllerian system is defined as the layer of tissue that lies underneath the mesothelial surface of the peritoneum. The proliferation of this mesenchyme may give rise to mesenchymal lesions composed of endometrial stromal-type cells, desidua, or smooth muscle.

Batt et al. suggested the theory of müllerianosis—developmentally misplaced Müllerian tissue—for their case [21]. In 2007, they defined müllerianosis by clinical-pathologic criteria as a heterotopic organoid structure of embryonic origin, a choristoma composed of Müllerian rests—normal endometrium, normal endosalpingeal tissue, and normal endocervical tissue—incorporated singly or in combination within other normal organs during organogenesis. He stated that Müllerian choristomas with only one Müllerian tissue, such as parauterine uterus-like mass, can be diagnosed with a high degree of probability only when three criteria are met: (1) no evidence of pelvic endometriosis, (2) no direct communication with the endocervix, endometrium, or endosalpinx, and (3) no history of surgery on the reproductive organs.

The differential diagnosis includes endometrioma with a smooth muscle component, leiomyomatosis peritonealis disseminata, extrauterine leiomyoma with entrapped endometrioid glands and stroma (adenomyotic leiomyoma), [2224], uterine malformation [9], and malignancy. The thick smooth muscle component distinguishes the mass from endometrioma and adenomyotic leiomyoma. The presence of cycling endometrium excludes leiomyomatosis peritonealis disseminata. Lack of atypia, mitosis, and necrosis in endometrial and smooth muscle component excludes malignancy.

Surgical treatment followed by long-term GnRH agonist therapy is said to be effective in keeping the disease stable [18]. As there are two reported extrauterine adenomyomas with features of uterus-like masses that occurred 17 and 22 years after hysterectomy, a long term followup is essential for these patients [16, 17]. Treatment with broad-based antibiotics can be unsuccessful for the abscessed ones.

The presence of ectopic adrenal tissue in the adnexal region is an interesting finding in our case. Although it was incidentally found, the development of this ectopic gland may be related to the development of uterus-like masses embryologically because the adrenal cortex develops from the coelomic mesodermal epithelium, that is closely related to Müllerian system, in the fourth to sixth week of gestation as a cluster of cells between the root of mesentery and the genital ridge [25]. Ectopic adrenal tissue can migrate with gonadal tissues. Therefore, adrenal rests can be found anywhere along the path of embryonic migration, including kidney, periadrenal, and retroperitoneal fat, in proximity to pelvic organs such as ovary, uterus, broad ligament, spermatic cord and vessels, and testes [26]. It is generally accepted that adrenal rests are due to mechanical separation and displacement of portions of cortical tissue during migration and descent of the sex glands. As coelomic epithelium is immediately adjacent to the developing Müllerian duct, a Müllerian duct fusion defect can cause mechanical separation of adrenal tissue.

In Schechter's report, Morgagni was said to be first described yellowish nodules resembling adrenal tissue adjacent to the main glands in 1740 [27]. Accessory glands are usually composed of cortical tissue only, and they are said to occur in 50% of newborns. They regress and disappear within a few years. In adults, they are generally found incidentally, in association with pelvic structures, such as the broad ligament, spermatic and ovarian vessels, spermatic cord, ovary, canal of Nuck, and uterus [26, 28].

The clinical implication, of the adrenal rests are essential in the surgical approach of the patients. In patients who have undergone bilateral adrenalectomy due to pathologic ACTH production, compensatory hyperplasia of the ectopic adrenal tissue may be responsible for the recurrence of the disease. Another clinical aspect is the possibility of formation and development of malignant disease in the ectopic gland.

Here we reported an interesting case with uterine and extrauterine abscessed adenomyomas with features of uterus-like masses. There was an ectopic adrenal tissue in the adnexal region. Although the ectopic tissue seems to be incidentally found, the development of these two separate entities may be related to each other embryologically.


  1. C. Zaloudek and M. R. Hendrickson, “Mesenchymal tumors of the uterus,” in Blaustein's Pathology of the Female Genital Track, R. J. Kurman, Ed., pp. 599–600, Springer, New York, NY, USA, 5th edition, 2002. View at Google Scholar
  2. A. Ferenczy, “Pathophysiology of adenomyosis,” Human Reproduction, vol. 4, no. 4, pp. 312–322, 1998. View at Publisher · View at Google Scholar · View at Scopus
  3. C. R. Martino, J. R. Haaga, and P. J. Bryan, “Secondary infection of an endometrioma following fine-needle aspiration,” Radiology, vol. 151, no. 1, pp. 53–54, 1984. View at Google Scholar · View at Scopus
  4. G. H. Lipscomb, F. W. Ling, and G. J. Photopulos, “Ovarian abscess arising within an endometrioma,” Obstetrics and Gynecology, vol. 78, no. 5, pp. 951–954, 1991. View at Google Scholar · View at Scopus
  5. R. Erguvan, M. M. Meydanli, A. Alkan, M. N. Edali, H. Gokce, and A. Kafkasli, “Abscess in adenomyosis mimicking a malignancy in a 54-year-old woman,” Infectious Disease in Obstetrics and Gynecology, vol. 11, no. 1, pp. 59–64, 2003. View at Publisher · View at Google Scholar · View at Scopus
  6. J. Rosai, “Uterus-corpus,” in Rosai and Ackerman's Surgical Pathology, J. Rosai, Ed., p. 1584, Mosby, St. Louis, Mo, USA, 9th edition, 2004. View at Google Scholar
  7. L. Choudhrie, N. N. Mahajan, M. V. Solomon, A. Thomas, A. J. Kale, and K. Mahajan, “Ovarian ligament adenomyoma: a case report,” Acta Chirurgica Belgica, vol. 107, no. 1, pp. 84–85, 2007. View at Google Scholar · View at Scopus
  8. S. Kaku, T. Moriya, N. Kanomata et al., “A case of extremely rare ovarian tumor: primary ovarian adenomyoma,” Kawasaki Medical Journal, vol. 37, no. 4, pp. 233–237, 2011. View at Google Scholar
  9. Y.-J. Liang, Q. Hao, Y.-Z. Wu, and B. Wu, “Uterus-like mass in the left broad ligament misdiagnosed as a malformation of the uterus: a case report of a rare condition and review of the literature,” Fertility and Sterility, vol. 93, no. 4, pp. 1347.e13–1347.e16, 2010. View at Publisher · View at Google Scholar · View at Scopus
  10. A. A. Ahmed, R. W. Swan, A. Owen, F. T. Kraus, and F. Patrick, “Uterus-like mass arising in the broad ligament: a metaplasia or mullerian duct anomaly?” International Journal of Gynecological Pathology, vol. 16, no. 3, pp. 279–281, 1997. View at Google Scholar · View at Scopus
  11. S. Matsuzaki, T. Murakami, S. Sato, T. Moriya, H. Sasano, and A. Yajima, “Endomyometriosis arising in the uterosacral ligament: a case report including a literature review and immunohistochemical analysis,” Pathology International, vol. 50, no. 6, pp. 493–496, 2000. View at Publisher · View at Google Scholar · View at Scopus
  12. C. J. R. Stewart, Y. C. Leung, R. Mathew, and A. L. McCartney, “Extrauterine adenomyoma with atypical (symplastic) smooth muscle cells: a report of 2 cases,” International Journal of Gynecological Pathology, vol. 28, no. 1, pp. 23–28, 2009. View at Publisher · View at Google Scholar · View at Scopus
  13. C. Cozzutto, “Uterus-like mass replacing ovary. Report of a new entity,” Archives of Pathology and Laboratory Medicine, vol. 105, no. 10, pp. 508–511, 1981. View at Google Scholar · View at Scopus
  14. D. Gurel, B. Tuna, and K. Yorukoglu, “Uterus-like mass of the ovary,” Turkish Journal of Pathology, vol. 23, no. 2, pp. 103–106, 2007. View at Google Scholar
  15. Y. Kaufman and A. Lam, “The pelvic uterus-like mass-A primary or secondary Müllerian system anomaly?” Journal of Minimally Invasive Gynecology, vol. 15, no. 4, pp. 494–497, 2008. View at Publisher · View at Google Scholar · View at Scopus
  16. R. Redman, E. J. Wilkinson, and N. A. Massoll, “Uterine-like mass with features of an extrauterine adenomyoma presenting 22 years after total abdominal hysterectomy-bilateral salpingo-oophorectomy: a case report and review of the literature,” Archives of Pathology and Laboratory Medicine, vol. 129, no. 8, pp. 1041–1043, 2005. View at Google Scholar · View at Scopus
  17. A. Khurana, A. Mehta, and M. Sardana, “Extrauterine adenomyoma with uterus like features: a rare entity presenting 17 years post hysterectomy,” Indian Journal of Pathology and Microbiology, vol. 54, no. 3, pp. 572–573, 2011. View at Publisher · View at Google Scholar · View at Scopus
  18. S. Carinelli, F. Motta, G. Frontino, E. Restelli, and L. Fedele, “Multiple extrauterine adenomyomas and uterus-like masses: case reports and review of the literature,” Fertility and Sterility, vol. 91, no. 5, pp. 1956.e9–1956.e11, 2009. View at Publisher · View at Google Scholar · View at Scopus
  19. G. Cranstoun, “Cystic adenomyoma of uterus,” Proceedings of the Royal Society of Medicine, vol. 15, pp. 8–9, 1922. View at Google Scholar
  20. T. Sadler, Langman's Medical Embryology, Williams and Wilkins, Baltimore, Md, USA, 6th edition, 1990.
  21. R. E. Batt, R. A. Smith, G. M. B. Louis et al., “Müllerianosis,” Histology and Histopathology, vol. 22, no. 10-12, pp. 1161–1166, 2007. View at Google Scholar · View at Scopus
  22. M. F. Lerwill, R. Sung, E. Oliva, J. Prat, and R. H. Young, “Smooth muscle tumors of the ovary: a clinicopathologic study of 54 cases emphasizing prognostic criteria, histologic variants, and differential diagnosis,” The American Journal of Surgical Pathology, vol. 28, no. 11, pp. 1436–1451, 2004. View at Publisher · View at Google Scholar · View at Scopus
  23. S. D. Billings, A. L. Folpe, and S. W. Weiss, “Do leiomyomas of deep soft tissue exist? an analysis of highly differentiated smooth muscle tumors of deep soft tissue supporting two distinct subtypes,” The American Journal of Surgical Pathology, vol. 25, no. 9, pp. 1134–1142, 2001. View at Publisher · View at Google Scholar · View at Scopus
  24. G. T. Kingston and S. Manek, “Endometrial glands and stroma within uterine smooth muscle proliferations: an introduction of the concept of an adenomyotic leiomyoma,” Histopathology, vol. 51, no. 5, pp. 721–723, 2007. View at Publisher · View at Google Scholar · View at Scopus
  25. E. E. Lack and J. A. Wieneke, “The adrenal glands,” in Urologic Surgical Pathology, D. G. Bostwick and L. Cheng, Eds., pp. 953–955, Mosby Elsevier, 2nd edition, 2008. View at Google Scholar
  26. J. Rosai, “Adrenal gland and other paraganglia,” in Rosai and Ackerman'a Surgical Pathology, J. Rosai, Ed., p. 1118, Mosby, St. Louis, Mo, USA, 9th edition, 2004. View at Google Scholar
  27. D. C. Schechter, “Aberrant adrenal tissue,” Annals of Surgery, vol. 167, no. 3, pp. 421–426, 1968. View at Google Scholar · View at Scopus
  28. J. R. Anderson and A. H. McLean Ross, “Ectopic adrenal tissue in adults,” Postgraduate Medical Journal, vol. 56, no. 661, pp. 806–808, 1980. View at Google Scholar · View at Scopus