Gestational trophoblastic neoplasia differential diagnosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Monalisa Dmello, M.B,B.S., M.D. [2]

Overview

Choriocarcinoma must be differentiated from non neoplastic diseases, neoplastic diseases, and other causes of bleeding during pregnancy.

Differentiating choriocarcinoma from other diseases

Choriocarcinoma must be differentiated from other non-neoplastic diseases such as:

Choriocarcinoma must be differentiated from other neoplastic diseases such as:

  • Invasive hydatidiform mole
  • Placental site trophoblastic tumor (PSTT)
  • Mixed germ cell tumor - esp. for testicular and ovarian tumors

Choriocarcinoma must be differentiated from other causes of bleeding during pregnancy:

Differential Diagnosis Clinical Features Karyotype Immunostaining Management
Presenting Complaints Potential for Neoplastic Conversion Beta Human Chorionic Gonadotropin (Beta-hCG) Baseline Levels History of Pregnancy Theca Leutin Cysts Metastatic Route Cytokeratin 18 HLA-G Human Chorionic Gonadotropin (hCG) Transformation-Related Protein 63 (P63) Human Placental Lactogen (hPL) Melanoma Cell Adhesion Molecule (Mel-CAM) Ki67
Complete Hydatidiform Mole
  • High rate of progression (15-20%)
  • Extremely high levels ( > 100000 mIU/ml in half of the patients
  • Not related
  • Present
  • Benign
  • 46, XX or 46 XY (Paternal dispermy)
  • Absent
  • Absent
  • Extremely elevated
  • Absent
  • Absent
  • Absent
  • Absent
  • Dilation and curettage (suction)
Partial Hydatidiform Mole
  • < 5 % progression rate
  • Highly elevated ( > 100000 mIU/ml in one in ten patients)
  • Not related
  • Absent
  • Benign
  • 69,XXY or XYY
  • Absent
  • Absent
  • Highly elevated
  • Absent
  • Absent
  • Absent
  • Absent
  • Dilation and curettage (suction)
Invasive Molar Pregnancy
  • High
  • Consequence of molar pregnancy
  • May be present
  • Hematogenous
  • 69,XXY or XYY
  • Positive
  • Positive
  • Highly elevated
  • Absent
  • Absent
  • Absent
  • Absent
Choriocarcinoma
  • Neoplastic
  • High
  • Present
  • Hematogenous
Placental-site Trophoblastic tumor (PSTT) and Epitheloid Trophoblastic Tumor (ETT)
  • Neoplastic
  • Moderatley elevated (< 1000 mIU/ml in majority of patients)
  • Absent
  • Lymphatic
  • 46,XX or XY
  • Positive
  • Positive
  • Negative (Positive in ETT)
  • Positive (Negative in ETT)
  • Positive (Negative in ETT)
  • Positive ( >1% in PSTT and >10% in ETT)
  • Hysterectomy
Ovarian Tumors[1][2][3][4][5][6][7][8][9]
  • Vagina bleeding or discharge
  • Weight loss
  • Urinary frequency/urgency
  • Change in bowel habits
  • Loss of appetite
  • Pelvic pressure/pain
  • Abdominal pain
  • Neoplastic
  • Elevated (Dysgerminoma and Embryonal carcinoma)
  • Overall incidence in pregnancy is 2.4-5.7% (1/300 to 1/556 pregnancies)
  • Incidence of malignancy is 1/15,000 to 1/32,000 pregnancies
  • Germ cell and epithelial tumors are most common
  • Absent
  • Direct extension or seeding
  • 46,XX
  • Absent (Epithelial tumors may be positive for cytokeratin AE1/AE3)
  • Positive
  • Elevated in dysgerminomas and embryonal carcinoma)
  • Positive (especially in epithelial cancers)
  • Positive
  • Positive
  • Positive
  • Surgical debulking
  • Intravenous/intraperitoneal chemotherapy
Spontaneous Abortion
  • Vaginal bleeding
  • Lower abdominal pain
  • Lower back pain
  • Vaginal passage of fetal tissue
  • Reduced uterine size and regression of signs and symtoms of pregnancy
  • Firm cervix
  • Not applicable
Ectopic Pregnancy
  • Abdominal/pelvic pain
  • Vaginal bleeding
  • Amenorrhea
  • Nausea
  • Syncope
  • Not applicable
Normal Term Pregnancy
Clinical Features Complete Hydatidiform Mole Partial Hydatidiform Mole Invasive Molar Pregnancy Choriocarcinoma Placental-site trophoblastic tumor (PSTT) and Epithelioid trophoblastic tumor (ETT)
Presenting Complaints
Neoplastic Conversion
Beta Human Chorionic Gonadotropin (Beta-hCG) baseline levels
  • High
  • High
History of Pregnancies
Metastatic Route
Management

References

  1. Farahmand SM, Marchetti DL, Asirwatham JE, Dewey MR (May 1991). "Ovarian endodermal sinus tumor associated with pregnancy: review of the literature". Gynecol. Oncol. 41 (2): 156–60. PMID 2050306.
  2. Hopkins MP, Duchon MA (November 1986). "Adnexal surgery in pregnancy". J Reprod Med. 31 (11): 1035–7. PMID 3806533.
  3. Lavery JP, Koontz WL, Layman L, Shaw L, Gumpel U (October 1986). "Sonographic evaluation of the adnexa during early pregnancy". Surg Gynecol Obstet. 163 (4): 319–23. PMID 3532382.
  4. Dgani R, Shoham Z, Atar E, Zosmer A, Lancet M (June 1989). "Ovarian carcinoma during pregnancy: a study of 23 cases in Israel between the years 1960 and 1984". Gynecol. Oncol. 33 (3): 326–31. PMID 2722058.
  5. Lengyel E (September 2010). "Ovarian cancer development and metastasis". Am. J. Pathol. 177 (3): 1053–64. doi:10.2353/ajpath.2010.100105. PMC 2928939. PMID 20651229.
  6. Goel A, Rao NM, Santhi V, Byna SS, Grandhi B, Conjeevaram J (2018). "Immunohistochemical Characterization of Normal Ovary and Common Epithelial Ovarian Neoplasm with a Monoclonal Antibody to Cytokeratin and Vimentin". Iran J Pathol. 13 (1): 23–29. PMC 5929385. PMID 29731792.
  7. Rebmann V, Regel J, Stolke D, Grosse-Wilde H (October 2003). "Secretion of sHLA-G molecules in malignancies". Semin. Cancer Biol. 13 (5): 371–7. PMID 14708717.
  8. Zhou P, Xiong T, Chen J, Li F, Qi T, Yuan J (February 2019). "Clinical significance of melanoma cell adhesion molecule CD146 and VEGFA expression in epithelial ovarian cancer". Oncol Lett. 17 (2): 2418–2424. doi:10.3892/ol.2018.9840. PMC 6341705. PMID 30675307.
  9. Mita S, Nakai A, Maeda S, Takeshita T (December 2004). "Prognostic significance of Ki-67 antigen immunostaining (MIB-1 monoclonal antibody) in ovarian cancer". J Nippon Med Sch. 71 (6): 384–91. PMID 15673959.