Minimal Laparotomy Management of a Giant Asymptomatic Ovarian Teratoma in a Woman of Reproductive Age: A Case Report

Ovarian tumors can originate from any of its different layers. The three major histological types are: epithelial tumors, sex cord stromal cell tumors, and germ cell tumors, which constitute approximately 25% of all ovarian tumors (Figure 1) [1].

Teratomas are slow-growing tumors, composed histologically of diverse tissues, such as bone, skin, sebaceous glands, etc., owing to its cell of origin. Pathologically, teratomas are classified into benign mature, malignant immature, and mono-dermal types that are composed of one type of tissue [2]. In 10-17% of cases, both ovaries are involved [3].

Ovarian teratomas rarely exceeds the diameter of 15cm. Teratomas that exceed this size have an increased likelihood of malignant transformation. Other risk factors include elevated tumor markers and advanced age [4]. Giant teratomas usually present with complications, including torsion, pressure symptoms, and rupture. Here, we report a rare case of an asymptomatic giant teratoma in a 32-year-old multiparous woman. The CARE guidelines were followed for this case report [5].

A 32-year-old multiparous woman was referred for further evaluation of a suspicious abdominal mass. During a discussion of the patient’s medical history, the patient admitted to the existence of this mass for more than one year in association with vague, intermittent abdominal pain. She reported no changes in her menstrual cycle or bowel habits. There was no other significant medical or family history. On inspection of the abdomen, a clear bulge was evident approximately 20×30cm in size in the periumbilical region. It was soft, and no area of tenderness could be detected (Figure 2).

Due to its huge size, an extensive workup was performed to assess the possible risks of malignancy. The levels of serum tumor markers α-fetoprotein (AFP), carcinoembryonic antigen (CEA), and β-human chorionic gonadotropin, were normal. However, the patient’s CA125 level was abnormally high at 50 U/ml (normal range, <35 U/ml). Abdominal contrast computed tomography (CT) revealed a 25×20×14cm pelviabdominal cystic multilocular mass with fluid/fat density and internal nodules of fat and calcific teeth (Rokitansky nodules) suggestive of a dermoid cyst, originating from the left ovary. Displacement of the surrounding bowel loops and diffuse anterior abdominal wall contour bulge were also noted (Figure 3). There was no evidence of enlarged lymph nodes, ascites, or tumor deposits in the abdomen or pelvis.

Other blood test findings were within the normal ranges, and liquid base cytology was negative for malignant cells. The radiological and laboratory findings were discussed in detail with the patient, and the possible risks of malignancy were highlighted. Written informed consent for surgery was obtained.

A mini-midline laparotomy was performed. A huge mass was seen originating from the left ovary, extending to the liver, with an approximate size of 20×40×20cm. The fallopian tube was stretched out by the mass. The cyst was aspirated completely without spillage in the peritoneal cavity. A total 5 L of thick, yellowish fluid was aspirated. No ascites or organ infiltrate was noted. Complete adenectomy was performed due to the absence of a cleavage line between the cyst and the ovary; the ovarian tissue was completely destroyed by the mass (Figure 4a). However, the contralateral tube and uterus were normal. The patient had an uneventful recovery and was discharged on the third post-operative day.

Histopathological assessment revealed a mature cystic teratoma composed of skin with appendages (Figure 4b), bone with marrow in addition to muscle tissues, nerve bundles, and glial tissues. Scarce ovarian tissue was included in a part of the cyst’s wall. No foci of malignant change could be detected. These findings were communicated to the patient post-operatively. A remarkable reduction in her weight by approximately 5 kg was noted during a visit to the clinic 10 days post-operation. In addition, she reported feeling light with an improved level of physical activity.

Although teratomas are common, reaching an abnormally huge size that exceeds 15 cm in diameter is rare. In a retrospective study conducted by Ayhan, et al. 501 operative patients’ records between 1964 and 1998 at Hacettepe University Hospital were examined, and the mean tumor diameter was 7.0±4.5 cm [6].

Teratomas are encountered in women of reproductive age, with rare cases having been reported at extreme ages. Asymptomatic giant teratomas are extremely rare because, since they occupy most of the abdominal-pelvic cavity, they will exert pressure on the surrounding structures or torsion, causing pressure/pain symptoms. Furthermore, over-stretching of the capsule with the collected material may amount to capsular rupture, chemical peritonitis, and dissemination of malignant cells, if present [7].

Although malignant transformation is rare, approximately 1-2% of teratoma cases become malignant [8]. Diagnosing malignancy in a giant cystic teratoma preoperatively is not easy. The role of elevated values of serum tumor markers is not fully understood; while some have reported that SCC Ag (squamous cell carcinoma antigen) is a useful marker to indicate squamous cell carcinoma in mature cystic teratomas, others found that CA125 and CA19-9 can be elevated in benign teratomas [3].

Ultrasonography has a very high positive predictive value in diagnosing ovarian teratomas, but it is limited in assessing the coexitance of metastasis. Therefore, additional CT scans or magnetic resonance imaging are required for optimum preoperative assessment of giant teratomas. Fat attenuation within a cyst with or without calcification is pathognomonic for mature cystic teratoma [9,10].

Surgical excision is fundamental to obtain a histopathological diagnosis and to detect the presence of immature elements. Both laparoscopic and open approach have been described to excise giant teratomas. However, the high possibility of spillage of teratoma contents is a procedure-related risk, which can be noted in up to 100% of laparoscopic surgery cases and 13% of laparotomy cases [11].

Spillage of the contents is associated with a substantial risk of chemical peritonitis and dissemination of malignant cells. The incidence rate of chemical peritonitis owing to granulomatous peritonitis is approximately 8% of cases [12]. Furthermore, prelaparoscopic decompression might be impractical in cases of solid teratomas. Further, using the laparoscopic approach for masses >10cm in size is debatable [13]. A retrospective study of 306 cases reported that laparoscopic surgery was performed in 57.8% (n=177) of patients, and cyst rupture occurred in 19 (6.2%) patients [8]. Shalev and Peleg recommended laparoscopic surgery as routine treatment for ovarian teratomas as large as 15cm in diameter [14]. Nevertheless, this is not recommended by many investigators, especially if malignancy is suspected [15]. Tsalkidou et al. performed an exploratory laparotomy in a 26-year-old woman with a huge benign cystic teratoma measuring 14×20×18cm who presented with progressive abdominal distension and discomfort five years after giving birth [15]. Further, Barghi, et al. performed a successful percutaneous drainage of 18.5 L of fluid followed by a mini-laparotomy for a 38×32×23cm mucinous ovarian cystadenoma in association with a mature cystic teratoma in a 26-year-old woman who had progressive abdominal distension over several years [16].

None.

Authors declare no conflict of interest.

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