Leukemoid reaction in cervical cancer: a case report and review of the literature
© Qing et al.; licensee BioMed Central Ltd. 2014
Received: 27 March 2014
Accepted: 8 September 2014
Published: 15 September 2014
The presentation of a leukemoid reaction in cervical cancers is rare. A leukemoid reaction is defined as leukocytosis associated with a cause outside the bone marrow, with the white blood cell count (WBC) exceeding 50*109/L. Two cervical cancers presenting with leukemoid reactions were previously reported. However, the cancers in these cases were mainly in the advanced stages and had a poor outcome.
Here we report a 40-year old patient with clinical stage (FIGO IIA1) cervical squamous carcinoma suffering from vaginal cuff recurrence with a leukemoid reaction two months after laparoscopic radical hysterectomy. The patient suffered from persistent fever and leukocytosis after one month of antibiotic treatment accompanied by rapid growth of the vaginal mass indicated that the leukocytosis could not be caused only by infection. After paclitaxel injection, the WBC count increased to 70.37*109/L. Bone marrow aspirates and biopsy showed left-shift neutrophilia, which confirmed leukemoid reaction. After two courses of paclitaxel and cisplatin treatment, the white blood cell counts decreased to normal, the fever disappeared, and the vaginal mass was reduced dramatically. She achieved completed remission after subsequent chemo-radiation and two additional courses of chemotherapy.
In our case, leukemoid reaction was related to recurrent cervical carcinoma and sensitive to chemotherapy. To our knowledge, this is the third case to be reported in the literature. Furthermore, this is the only case described that shows an unequivocal correlation between tumor response and leukemoid reaction.
KeywordsLeukemoid reaction Cervical cancer
Cervical cancer is the third most common cancer and the fourth leading cause of cancer death in women worldwide, and more than 85% of cases occur in developing countries . Clinically, the primary treatment for early stage cervical cancer is surgery, radiation therapy, or concurrent chemoradiation. The 5-year survival rate for early stage cervical cancer is 70% .
A white blood cell count (WBC) exceeding 50*109/L associated with a cause outside the bone marrow is termed a leukemoid reaction (LR). LR is generally benign, although it could resemble more serious conditions that are medical dilemmas. Its frequency in patients with nonhematologic cancers remains unclear, although it has been reported to range from 1% to 4% in small case series. LR has been reported in nearly all solid tumor types as a paraneoplastic syndrome and is historically associated with poor outcome. Cervical cancers presenting with LR are rarely reported. Only two authors, Nimieri  and Kyo , have reported LR in cervical cancer patients. However, the cancers in these cases were mainly in advanced stage. Here, we report a patient with relatively early stage (International Federation of Gynecology and Obstetrics, FIGO IIA1) cervical squamous carcinoma suffering from recurrence with LR two months after laparoscopic radical hysterectomy. The clinical and histological features are described. The literature describing these rare cases is also reviewed.
On July 2, 2012 (68 days after the operation), she presented to the outpatient clinic with increasing discharge. A 2*3 cm swollen cystic area was found in the posterior vagina. As purulent cells were found in her vaginal discharge, she was diagnosed with vaginitis and prescribed ornidazole to control the infection. On July 16, 2012, due to a high fever of 39.2°C and urine retention, she went to the urological outpatient clinic to receive catheterization. With a white blood cell count of 23*109/L, she was diagnosed with a urinary tract infection and received intravenous cefotiam and levofloxacin. However, her fever was not well controlled. On July 30, 2012, a 60 mm diameter solid mass on the posterior vagina with an ulcerous surface was found by gynecological examination. MRI scan confirmed a homogeneous solid 68*63*58 mm mass located in the space between the bladder and the rectum (Figures 1B and 4). MRI well displayed the tumor itself and its margin. After injection of contrast materials, the relationship between the tumor and surrounding tissues also was well appreciated on serial MRI scans. Hydronephrosis of both kidneys and distension of upper region of the left ureter were confirmed by ultrasonic inspection. Biopsy was performed on the mass, which demonstrated degenerated squamous cells within necrotic tissue.
She was admitted to the inpatient ward again on August 2. 2012. Because of an uncontrollable fever (range: 39–40.5°C) and leukocytosis (WBC: 29.66*109/L), samples of her blood, urine, and vaginal discharge were taken for bacterial culture to identify the source of infection. The cultures were all negative on August 2, 2012; however, Escherichia Colli, ESBLs (extended-spectrum β-Lactamase) sensitive to tienam and amikacin were found in a vaginal bacterial culture on August 5, 2012. Repeated discharge culture on August 12, 2012 was negative and became ESBLs positive again on August 17, 2012, then turned to negative on August 29, 2012. Since admission, empiric therapy with ceftriaxone sodium and metronidazole had been used; however, this was subsequently changed to a combination of tienam and vancomycin according to a drug sensitivity test on Aug 5, 2012. From August 12, 2012 to August 24, 2012, the patient was treated with norvancomycin and cefoperazone-sulbactam and subsequently with piperacillin-tazobactam plus amikacin for an additional 7 days.
On the other hand, although a biopsy on July 30, 2012 showed no malignancy (the possible negative result might be attributed to superficial biopsy sample), the recurrence of cervical carcinoma was highly suspected because the vaginal mass increased from 22*33*22 mm on July 2, 2012 to 63*65*58 mm on July 30, 2012 and the characteristics showed by MRI highly suggested a recurrent tumor. The tumor mass increased to 80 mm in diameter by palpation on August 6, 2012. A second bulky biopsy was performed on August 7, 2012. In order to get enough tissue, we cut the surface open, and excised a 60*40*20 mm mass. The whole mass was solid without abscess. After the biopsy, the tumor volume shrank to 70*40*40 mm. Pathology examination confirmed recurrent squamous carcinoma. Immunochemistry staining for Ki-67 and P53 was also performed (Figure 3). Chemotherapy was considered but was postponed because the patient was recently given sensitive antibiotics (tienam and vancomycin) and effective control of fever and leukocytosis was expected. However, one week later, the high fever (up to 39.2°C) and leukocytosis (up to 33.4*109/L) were persistent. In addition, the mass continued growing to 90*82*74 mm on August 14, 2012 and tumor makers became abnormal (CA125: 76.66 U/L, SCCA: 5.3 ng/ml). Considering the severity of the situation, we decided to give the patient a new regimen of antibiotics and chemotherapy simultaneously.
Regarding chemotherapy, paclitaxel (200 mg) was administered intravenously on August 15, 2012. Unexpectedly, on the following day, her fever increased (40.3°C), and the planned cisplatin treatment was cancelled. On August 21, 2012, cisplatin (100 mg) was injected because the patient had become relatively stable (fever, 39°C; WBC, 18.95*109/L). On August 25, 2012, her WBC count reached 70.37*109/L, and a leukemoid reaction (LR) was suspected. Bone marrow aspirates and biopsy showed an increased myeloid/erythroid ratio, active myeloid proliferation, and normal megakaryocytopoiesis. Meanwhile, her LAP level was extremely high (869 U/L). Considering the lab tests, the diagnosis of LR was established. On August 28, 2012 (12 days after paclitaxel and 1 week after cisplatin injection), her WBC count was reduced to 39.23*109/L, the mass was reduced to 65*46*40 mm, and SCCA and CA125 had decreased to 1.0 ng/ml and 49.46 U/L, respectively. On September 4, 2012 (three weeks after paclitaxel treatment), her fever and WBC count decreased to normal levels (36.8°C and 8.1*109/L). Subsequently, the levels of tumor markers returned to normal. The second course of paclitaxel (210 mg) and cisplatin (120 mg) was administered on September 10, 2012 and the vaginal mass was successfully eliminated on September 17, 2012. Additionally, after chemotherapy was performed, ultrasound results indicated that the kidney and IVP were normal. The dynamic changes in WBC, LAP, tumor makers, and tumor volume along with the chemotherapy are illustrated in Figure 2.
From October 10, 2012 to November 16, 2012, the patient received external irradiation to a dose of 45 Gy in 25 fractions with concurrent cisplatin chemotherapy. No abnormality was observed on MRI on November 19, 2012. After radiotherapy, she was treated with chemotherapy (100 mg docetaxel together with 300 mg carboplatin) on December 17, 2012 and January 14, 2013. The follow-up was satisfying: her WBC, CA125, and SCCA levels were normal. The latest follow-up on May 23, 2014 showed no evidence of recurrence.
The possible cause of LR in cancer patients
As in many other carcinomas, we considered LR as a paraneoplastic syndrome associated with cancer and attributed to increased cytokine production. Fever is an integral component of leukemoid reaction resulting from either release of endogenous pyrogens or due to necrotic-inflammatory phenomena of the tumor. Various studies have reported elevations in granulocyte colony-stimulating factor (G-CSF), granulocyte-macrophage colony-stimulating factor (GM-CSF), and interleukin-6 (IL-6) in tumors of the cervix, pancreatic cancer, hepatocellular carcinoma, and lung cancer [4, 6–8]. Animal experiments have demonstrated that interleukin-6 (IL-6) can sustain neutrophil/macrophage colonies in vivo and that, through its action on other immune cells, it can induce the production of several CSFs by the bone marrow . Despite stimulating bone marrow to sustain leukocytosis, IL-3, GM-CSF, and G-CSF have been shown to stimulate the growth of clonogenic cells of some nonhematopoietic malignant cell lines in vitro. Hurtado et al. found that when G-CSF was overproduced by tumor cells, it had a tendency to encourage the development of myeloid-derived suppressor cells (MDSC), which could travel to lymph nodes to prevent dendritic cell-primed T lymphocytes from eliminating tumor cells . Therefore, consistent with the clinical presentation of our case, paraneoplastic granulocytosis is often associated with rapid tumor growth and poor clinical prognosis, although it resolves with the treatment of the underlying cancers. Especially when infection is not likely or not the only contributor, the possibility of tumor origin should be considered when patients present with an LR of unknown etiology. Nevertheless, drugs that induce LRs, such as methotrexate  and carbamazepine , should be avoided.
The pathological characteristics of cancers with LR
Although we did not measure the G-CSF, GM-CSF, or IL-6 in the tumor cells, we compared the HE sections and several immunochemical markers in primary and recurrent tumors to investigate the possible factors related to the unusual presentation in our case. Based on Figure 2, there were more neutrophils in the tissue after the recurrence than before the recurrence, although the primary lesion had more neutrophils than usual. The infiltration of the tumor by neutrophil granulocytes and lymphocytes proved to be significant for prognosis and discrimination . A large number of neutrophils and lymphocytes in a cancerous lesion may be a clue indicating the potential for rapid recurrence. Nevertheless, Carus et al. recently assessed tumor-associated CD66b(+) neutrophils and CD163(+) macrophages by immunohistochemistry in whole tissue sections of 101 FIGO IB and IIA cervical cancer patients and found tumor-associated neutrophil count was an independent prognostic factor for short recurrence free survival in localised cervical cancer . The Ki-67 index, a marker of cell proliferation, is similarly associated with tumor recurrence and prognosis. A 90% positive Ki-67 score in a primary lesion might be an indicator of rapid recurrence. P53, which is often associated with poor prognosis, was also remarkably positively expressed in primary and recurrent tumors.
Treatment strategies for patients with LR
Treatment strategies for cancer with LR are limited and are rarely reported in the literature. As Granger and Kontoyiannis reported in a retrospective, single-institution study, patients who survived longer than 1 year received effective antineoplastic therapy, chemotherapy, or surgery. However, these authors did not mention specific strategies . The majority of malignant tumors with LR respond poorly to chemotherapy, and the patients die shortly after. For example, a lung cancer patient with LR treated with various drugs, including vinorelbine, cisplatin, docetaxel, pemetrexed, and gemcitabine died two weeks after starting third-line therapy . In our case, we used paclitaxel combined with cisplatin to control the development of LR. Surprisingly, after two courses of chemotherapy, the very large recurrent tumor completely disappeared and the WBC count decreased to normal. Subsequently, the patient received concurrent chemo-radiation therapy and an additional two courses of docetaxel combined with carboplatin. The patient survived for longer than 20 months after recurrence.
Prognosis of tumor patients with LR
Pathoclinical features in three cases of cervical cancer with LR
Time to recurrence
Radical hysterectomy, bilateral salpingo-oophorectomy, and pelvic lymphadenectomy
Right parametrial space
68 days after surgery, DOD$
Chemotherapy and local radiotherapy
Chemotherapy, local radiotherapy
6 weeks, DOD
laparoscopic radical hysterectomy, pelvic lymphadenectomy, vaginoplasty, and ovarian transposition
Chemotherapy + radiation
20 months, Alive
To our knowledge, this is the first case report of an early stage cervical cancer suffering rapid recurrence with leukemoid reaction achieving a good prognosis due to early diagnosis and timely chemotherapy. Unusual infiltration of the tumor by neutrophil granulocytes and high expression of Ki-67 and P53 may relate to rapid recurrence and leukemoid reaction.
Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
We thank Sarah C. and Lee L. who provided editing services on behalf of American Journal Experts.
- Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D: Global cancer statistics. CA Cancer J Clin. 2011, 61 (2): 69-90. 10.3322/caac.20107.View ArticlePubMedGoogle Scholar
- Singh P, Tripcony L, Nicklin J: Analysis of prognostic variables, development of predictive models, and stratification of risk groups in surgically treated FIGO early-stage (IA-IIA) carcinoma cervix. Int J Gynecol Cancer. 2012, 22 (1): 115-122. 10.1097/IGC.0b013e31822fa8bb.View ArticlePubMedGoogle Scholar
- Nimieri HS, Makoni SN, Madziwa FH, Nemiary D: Leukemoid reaction response to chemotherapy and radiotherapy in a patient with cervical carcinoma. Ann Hematol. 2003, 82 (5): 316-317.PubMedGoogle Scholar
- Kyo S, Kanaya T, Takakura M, Inoue M: A case of cervical cancer with aggressive tumor growth: possible autocrine growth stimulation by G-CSF and Il-6. Gynecol Oncol. 2000, 78 (3 Pt 1): 383-387.View ArticlePubMedGoogle Scholar
- Berdel WE, Danhauser-Riedl S, Steinhauser G, Winton EF: Various human hematopoietic growth factors (interleukin-3, GM-CSF, G-CSF) stimulate clonal growth of nonhematopoietic tumor cells. Blood. 1989, 73 (1): 80-83.PubMedGoogle Scholar
- Qureshi KM, Raman AK, Tan D, Fakih MG: Leukemoid reaction in pancreatic cancer: a case report and review of the literature. JOP. 2006, 7 (6): 631-634.PubMedGoogle Scholar
- Jain P, Roop RR, Jha A: Hepatocellular carcinoma manifesting as cavitary lung metastases and leukemoid reaction. J Gastrointestin Liver Dis. 2008, 17 (3): 355-356.PubMedGoogle Scholar
- Shalom G, Sion-Vardy N, Dudnik J, Ariad S: Leukemoid reaction in lung cancer patients. Isr Med Assoc J. 2010, 12 (4): 255-256.PubMedGoogle Scholar
- Hurtado-Cordovi J, Avezbakiyev B, Frieri M, Freedman L, Gebre W: Cutaneous inflammatory malignant fibrous histiocytoma presenting with a leukemoid reaction: a case report and review of the literature. Case Report Med. 2012, 2012: 798629-Google Scholar
- Hurtado-Cordovi J, Pathak P, Avezbakiyev B, Frieri M: Inflammatory malignant fibrous histiocytoma associated with leukemoid reaction or leukocytosis: a comprehensive review. ISRN Oncol. 2012, 2012: 946019-PubMedPubMed CentralGoogle Scholar
- Sun CY, Lin HC, Chen YC, Tsai CR, Wu MS: Leukemoid reaction after methotrexate-induced pancytopenia in a patient undergoing continuous ambulatory peritoneal dialysis. Chang Gung Med J. 2006, 29 (5): 513-517.PubMedGoogle Scholar
- Laad G, Miranda MF: Eosinophilic leukemoid reaction associated with carbamazepine hypersensitivity. Indian J Dermatol Venereol Leprol. 2005, 71 (1): 35-37. 10.4103/0378-6323.13784.View ArticlePubMedGoogle Scholar
- Stosiek P, Kasper M, Varga A: Relevant prognostic results in stomach cancer (analysis of variance and discriminance with clinical, morphologic and immunologic features). Arch Geschwulstforsch. 1983, 53 (1): 61-67.PubMedGoogle Scholar
- Carus A, Ladekarl M, Hager H, Nedergaard BS, Donskov F: Tumor-associated CD66b + neutrophil count is an independent prognostic factor for recurrence in localised cervical cancer. Br J Cancer. 2013, 108 (10): 2116-2122. 10.1038/bjc.2013.167.View ArticlePubMedPubMed CentralGoogle Scholar
- Granger JM, Kontoyiannis DP: Etiology and outcome of extreme leukocytosis in 758 nonhematologic cancer patients: a retrospective, single-institution study. Cancer. 2009, 115 (17): 3919-3923. 10.1002/cncr.24480.View ArticlePubMedGoogle Scholar
- Riesenberg H, Muller F, Gorner M: Leukemoid reaction in a patient with adenocarcinoma of the lung: a case report. J Med Case Rep. 2012, 6 (1): 211-10.1186/1752-1947-6-211.View ArticlePubMedPubMed CentralGoogle Scholar
- Ma X, Li G, Cai Z, Sun W, Liu J, Zhang F: Leukemoid reaction in malignant bone tumor patients - a retrospective, single-institution study. Eur Rev Med Pharmacol Sci. 2012, 16 (14): 1895-1899.PubMedGoogle Scholar
- Mabuchi S, Matsumoto Y, Isohashi F, Yoshioka Y, Ohashi H, Morii E, Hamasaki T, Aozasa K, Mutch DG, Kimura T: Pretreatment leukocytosis is an indicator of poor prognosis in patients with cervical cancer. Gynecol Oncol. 2011, 122 (1): 25-32. 10.1016/j.ygyno.2011.03.037.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/14/670/prepub
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