Open Journal of Pathology
Vol.08 No.04(2018), Article ID:87470,7 pages
10.4236/ojpathology.2018.84015

Anatomo-Clinical Case: Coexistence of Tuberculosis with Axillary Lymph Node Metastasis in Breast Carcinoma

Aimé Sosthène Ouédraogo1,2*, Hierrhum Aboubacar Bambara3, Franck Auguste Hermann Ademayali Ido1, Welbnoaga Norbert Ramdé2,4, Rimwaogdo Jeremie Sawadogo5, Ibrahim Savadogo6, Souleymane Ouattara7, Hassami Barry1, Assita Sanou-Lamien2,8, Olga Melanie Lompo2,8

1Pathological Anatomy Unit of Bogodogo District Hospital, Ouagadougou, Burkina Faso

2University Department of Research and Training in Health Sciences (UFR/SDS), Ouagadougou, Burkina Faso

3Clinical Oncology and Hematology Unit of Bogodogo District Hospital, Ouagadougou, Burkina Faso

4Legal Medicine Unit of Bogodogo District Hospital, Ouagadougou, Burkina Faso

5MD, MPH, CPH Research Institute, JPS Health Network, Fort Worth, TX, USA

6Pathological Anatomy Unit of Ouahigouya Regional Hospital Centre, Ouagadougou, Burkina Faso

7Pathological Anatomy Unit of Blaise Compaoré University Hospital Centre, Ouagadougou, Burkina Faso

8Yalgado Ouedraogo University Hospital Centre, Ouagadougou, Burkina Faso

Copyright © 2018 by authors and Scientific Research Publishing Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY 4.0).

http://creativecommons.org/licenses/by/4.0/

Received: August 2, 2018; Accepted: September 22, 2018; Published: September 25, 2018

ABSTRACT

Introduction: The coexistence of tuberculosis with axillary lymph node metastasis in breast carcinoma is uncommon. Observation: We report a case of a patient aged 59 years presenting a painless nodule in the right breast for one year. The scan and mammography revealed a long-axis node of 3 × 2 × 1 cm in the upper outer quadrant of the right breast ranked stage IV by the American College of Radiology (ACR), associated with a set of axillary lymph nodes and the largest one measuring 15 × 15 × 20 millimeters (mm). The breast biopsy helped diagnose a Scarff Bloom Richardson (SBR) grade II non-specific invasive carcinoma, modified by Ellis and Elston. A right mastectomy associated with a lymph node dissection was performed. We noticed a not well defined and whitish 5 mm tumor mass associated with 16 lymph nodes removed. The histological examination confirmed the diagnosis of SBR grade II non-specific invasive carcinoma with invasion of 7 lymph nodes (N+ = 7/16). In 3 metastatic lymph nodes, there were epithelioid and gigantocellular granulomas with full central necrosis. The Ziehl Neelsen staining had highlighted acid-fast bacilli. The tumor was oestrogen and progesteron receptor, without an overexpression of the oncoprotein human epidermal growth factor receptor 2 (HER2), which corresponds to a 0 score and the Ki 67 proliferation index assessed at 10%. The patient was given an anti-tuberculosis treatment combining Rifampicin (H), Isoniazid (I), Pyrazinamid (Z), Ethambutol (E) over 2 months and secondly a combination of Rifampicin and Isoniazid over 4 months (2RHZE/4 RH). The anti-tumor chemotherapy used a protocol combining 3 FAC60+ 3 Docetaxel (F = Fluorouracil®; A = Adriblastin®, C = Cyclophosphamid). Conclusion: This coexistence is uncommon, of incidental discovery and necessitates a multidisciplinary care.

Keywords:

Breast Carcinoma, Tuberculosis, Lymph Node, Histopathology

1. Introduction

The coexistence of breast cancer and tuberculosis is very uncommon and less reported in the literature [1] [2] [3] [4] [5] . The clinical features of mammary tuberculosis may reveal nodules and ulcerations with the appearance of lymphadenopathies leading us to suspect a malign tumor. It is the histological examination that enabled making the differential diagnosis. We report an uncommon case of non-specific infiltrating breast carcinoma with metastatic homolateral lymph node associated with lymph node tuberculosis that was incidentally discovered during the histological examination.

2. Anatomo-Clinical Case

We report the case of a patient of 59 years, 7 pregnancies, 5 parities, menopausal since 12 years, without cancer disease history in her family, who presented a painless and moving nodule discovered in the right breast after a self-breast examination. The nodule had been evolving for one year. The scan and mammography revealed a nodule of 3 × 2 × 1 cm in the upper outer quadrant of the right breast ranked ACR IV, associated with a group of axillary lymph nodes including the largest one measuring 15 × 15 × 20 mm. A breast biopsy had helped diagnose a Scarff Bloom Richardson (SBR) grade II non-specific invasive breast carcinoma, modified by Ellis and Elston.

A right mastectomy associated with a lymph node dissection was performed and presented a not well defined and whitish 5 mm tumor mass of large axis with 16 lymph nodes.; the largest one was measuring 3 cm.

The histological examination had confirmed the diagnosis of SBR grade II non-specific invasive breast carcinoma with an invasion of 7 lymph nodes over 16 (N+ = 7/16). In 3 metastatic lymph nodes, there were epithelioid and gigantocellular granulomas centered by a full necrosis (Figure 1 and Figure 2). The Ziehl Neelsen staining had highlighted acid-fast bacilli (AFB) (Figure 3). There were no vascular emboli or peripheral nerve sheathing.

The immunohistochemistry examination carried out in paraffin section had revealed a high expression of estrogen and progesterone receptors assessed at

Figure 1. Breast carcinoma and lymph node tuberculosis. Hematein Eosin (HE) stain, Magnification ×100. Carcinomatous proliferation (star) infiltrating a lymph node parenchyma which is the site of a granulomatous inflammatory reaction with central necrosis (arrow).

Figure 2. Breast carcinoma and lymph node tuberculosis. Hematein Eosin (HE) stain, Magnification ×100. Granulomatous inflammatory reaction with complete central necrosis (star) and giant Langhans cells (arrow).

Figure 3. Breast carcinoma and lymph node tuberculosis. Hematein Eosin (HE) stain, Magnification ×100 and in cartridge Zielh Neelsen staining. Carcinomatous proliferation infiltrating a lymph node parenchyma which is the site of a granulomatous inflammatory reaction with central necrosis and highlight of Acid-Fast Bacilli (AFB) with Zielh Neelsen staining (cartridge).

90% each (Figure 4 and Figure 5), without an overexpression of the oncoprotein HER2 (Score 0). The Ki 67 proliferation index was assessed at 10% (Figure 6).

The patient was submitted to an anti-tuberculosis treatment associated with a chemotherapy protocole made up of 3 FAC 60 +3 Docetaxel. The FAC60 protocol followed by the Docetaxel protocol was given on a regular interval of 21 days at the same time with the anti-tuberculosis protocol: 2RHZE/4 RH (R = Rifampicin; H = Isoniazid; Z = Pyrazinamid; E = Ethambutol). The major side

Figure 4. Breast carcinoma and lymph node tuberculosis. Immunohistochemistry Magnification ×400. Intense and diffuse immunostaining with anti-estrogen receptor (RO) antibodies relevant to tumor cell nuclei.

Figure 5. Breast carcinoma and lymph node tuberculosis. Immunohistochemistry Magnification ×400. Intense and diffuse immunostaining with anti-progesterone receptor (RP) antibodies relevant to tumor cell nuclei.

Figure 6. Breast carcinoma and lymph node tuberculosis. Immunohistochemistry Magnification ×400 (H & E). Moderate and diffuse immunostaining with anti-Ki 67 antibody showing a proliferation index evaluated at 10%.

effect was a clinical anemia with a hemoglobin rate at 10.5 g/ml. This anemia was contained through the administering of anti-anemia drugs. The patient is at her 5th chemotherapy cycle.

3. Discussion

The coexistence of breast cancer and tuberculosis is very uncommon and less reported in the literature. This coexistence raises difficulties in the diagnostic and therapeutic care [3] . The first case was described in 1899 by Wharti, later followed by other authors [6] . The prevalence is estimated at 19/10,000 according to the data in the literature [7] . Extra-pulmonary tuberculosis most often localizes in cervical, inguinal and axillary lymph nodes, but the coexistence with a cancer is very rare and of incidental discovery [6] . The histological examination of the removed lymph nodes revealed a non-specific invasive breast carcinoma associated with an epithelioid and gigantocellular granuloma with full central necrosis which is characteristic of tuberculosis. The giant cells are of Langhans type (Figure 2). The Ziehl Nielsen staining often highlighted AFBs (Figure 3). The histology enabled determining the conventional prognosis factors, especially the Nottingham score (SBR grade II), the number of lymph nodes invaded over the total number of lymph nodes removed (N+ = 7/16) and the presence of vascular emboli. Other prognostic and therapeutic factors are determined by the immunohistochemistry with the dosage of estrogen (RO) and progesterone (RP) receptors, the HER2 oncoprotein and the Ki67 proliferation index. These elements have helped establish a molecular classification of the tumor as Luminal A (RO+, RP+, HER2-, Ki67 inferior to 14% [8] .

The patient was submitted to an anti-tuberculosis treatment associated with a chemotherapy protocol. The anti-tuberculosis protocol is based on polychemotherapy. The first-line drugs of tuberculosis used by the National Tuberculosis Plan (PNT) of Burkina Faso are five in number: Isoniazid H, Rifampicin R, Streptomycin S, Ethambutol E, Pyrazinamid Z.

The treatment is made up of two phases. An initial phase of treatment or intensive phase comprises four drugs that are Ethambutol (E), Rifampicin (R), Isoniazid (H) and Pyrazinamid (Z). The advantage of this phase is that it is very efficient in reducing bacilli and the resistance to anti-tuberculosis drugs. It takes two or three months. The continuation phase is necessary for the patient’s final recovery. It helps avoid the recurrence of tuberculosis when the treatment is stopped. It required 2 drugs over a period of four months.

Tolerance and compliance with the treatment were good. They were regularly assessed through the Directly Observed Therapy (DOT) strategy. This strategy is recommended by WHO and consists in giving the drugs under control or verifying at least 3 times a week if they are effectively taken.

Chemotherapy is used as adjuvant and involves the 3 FAC + 3 Docetaxel protocol. It is currently recommended to give it before the radiotherapy. The treatment usually takes six months.

Our patient did not benefit from radiotherapy and hormonotherapy, due to the lack of financial means. The 2 protocols (anti-tuberculosis treatment and chemotherapy) were given at the same time. There is no consensus over the simultaneous or separated combination of these two protocols. Anti-tuberculosis treatment is a determining factor in cancer prognosis and evolution. Thus, anti-bacilli treatment must be initiated once the diagnosis is made, as there is a risk for the occurrence of serious forms of tuberculosis (miliary and meningitis tuberculosis) as the consequence of the immunodepression caused by the anti-cancer treatment [9] . However, the combination of the anti-tuberculosis treatment with anti-cancer chemotherapies may entail a multiplication of the risk of adverse effects through an exacerbation of toxicities or a modification in the efficiency of the anti-cancer treatment 10]. The side effect noted was a clinical anemia with a hemoglobin rate at 10.5 g/dl, addressed through an anti-anemia treatment.

The evolution still remains favourable without recurrence of cancer or the appearance of a tuberculosis disease.

4. Conclusion

This coexistence is uncommon and of incidental discovery, hence there is a need for a careful and full examination of lymph node dissections. The treatment requires a multidisciplinary collaboration.

Conflicts of Interest

The authors declare no conflict of interest.

Cite this paper

Ouédraogo, A.S., Bambara, H.A., Ido, F.A.H.A., Ramdé, W.N., Sawadogo, R.J., Savadogo, I., Ouattara, S., Barry, H., Sanou-Lamien, A. and Lompo, O.M. (2018) Anatomo-Clinical Case: Coexistence of Tuberculosis with Axillary Lymph Node Metastasis in Breast Carcinoma. Open Journal of Pathology, 8, 132-138. https://doi.org/10.4236/ojpathology.2018.84015

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