International Journal of Scientific Reports

Malik P et al. Int J Sci Rep. 2016 Jul;2(7):165-167

http://www.sci-rep.com

pISSN 2454-2156 | eISSN 2454-2164

Primary hydatid cyst of intercostal muscles: a rare entity

Preeti Malik1*, Karamveer Singh2


1Pt. B.D. Sharma, Post graduate Institute of Medical Sciences, Rohtak, Haryana, India

2Department of General Surgery, General Hospital, Bahadurgarh, Jhajjar, Haryana, India

Received: 09 May 2016

Accepted: 08 June 2016

*Correspondence:

Dr. Preeti Malik

E-mail: dr.priti.malik@gmail.com

Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

ABSTRACT

Usually intramuscular hydatid cysts are secondary, resulting from other areas either spontaneously or after surgery for hydatidosis in other regions. We present an unusual case of a primary hydatid cyst found in left chest wall of a 38-year-old woman, presenting as an enlarging soft tissue lump with pain which was diagnosed intraoperatively.

Keywords: Hydatid cyst, Muscular echinococossis

INTRODUCTION

Echinococossis is an infectious disease caused by the cestode Echinococcus commonly affecting liver and lungs. Isolated muscular hydatid cyst is a rare entity. We are reporting a case of primary hydatid disease in left lower intercostal muscles. Such cases are rarer in literature.

CASE REPORT

A 38 year old female presented in Surgery Department, General Hospital, Bahadurgarh, Jhajjar, Haryana, India, with a slowly enlarging painful lump of 4 months duration in left lower chest anterior to mid axillary line at the level of 10th rib. On clinical examination, the lump was tender on palpation with restricted mobility (not freely mobile). Earlier, the patient had undergone an incomplete course (2 months) of antitubercular and other medical treatments for similar complaints from various hospitals but was not diagnosed and relieved. Patient was screened for tuberculosis via serological, radiological and sputum examinations, Mantoux test, neither of which suggested tuberculosis as etiology. FNAC of the lesion was reported as a lipoma. Patient was explored after informed consent under local anaesthesia for surgery.

Figure 1: Incision showing pearly white hydatid cyst.
Figure 1: Incision showing pearly white hydatid cyst.

On dissection, beneath the subcutaneous fat, a lump was palpable. On further dissection and retraction of intercostal muscles, a cystic lesion was visible, the aspiration of which revealed clear fluid. On opening the cystic cavity, pearly white membranes were seen in the cyst along with the clear fluid suggesting diagnosis of hydatid cyst. The lesion was isolated with 10% povidone iodine soaked gauze for 10 minutes and the cyst was closed after aspiration (due to unknown extent of the lesion). The wound was washed with 10% povidone iodine and was sutured to be re-explored later after CT scan of thorax. Patient was kept under observation for 24 hours post exploration for anaphylaxis/untoward incident and tablet albendazole 400 mg twice a day along with antibiotic cover was started. The definitive surgery was done later under general anaesthesia after knowing the extent and location of hydatid cyst.

Figure 2: Computed tomography (arrow) showing hydatid cyst in intercostal muscles.
Figure 2: Computed tomography (arrow) showing hydatid cyst in intercostal muscles.

DISCUSSION

Hydatidosis is an infectious disease caused by the tapeworm of the genus Echinococcus granulosus, E. multilocularis and E. oligarthus. E. granulosus is the most common cause of hydatid disease.1 Contamination of human beings (intermediate host) occurs accidentally through contact with dogs (definitive host) or by the ingestion of food or drink containing the larval stages of the parasitic tapeworm. It is endemic in the Middle East and other parts of the world including India, Africa, South America, New Zealand, Australia, Turkey and Southern Europe.2-4 Infestation by hydatid disease in human beings most commonly occurs in the liver (55-70%) followed by the lung (18-35%). The two organs can be affected simultaneously in about 5-13% cases.5,6 It can also affect the brain, heart, kidney, ureter, spleen, uterus, fallopian tube, mesentery, pancreas, diaphragm and muscles.7

One report from Turkey described a hydatid cyst in the adductor muscle group.8 Abdel-Khaliq described pectoralis major muscle involvement.9 Pouche et al showed hydatid cysts in rectus and back muscles.10

Primary hydatid disease of the skeletal muscle is rare, as the parasite has to cross pulmonary and hepatic barriers to reach the muscles.11 The high lactic acid level in muscle tissue is considered unfavorable for the survival of parasite.12

Classically the patient presents with a long history of cystic lump with muscle fixation. Although eosinophilia is expected in patients with parasitic infestations, this may not always be seen.13 Pre-operative diagnosis can be made on ultrasound, CT, or MRI by the characteristic appearance of a unilocular or multilocular cyst with multiple daughter cysts.

Surgery is the optimal treatment of hydatid disease and thorough irrigation of the cystic cavity with scolicidal agents (exposure time) like hydrogen peroxide 3% (15 minutes), hypertonic saline 15-30% (10 minutes), povidone iodine 10% (10 minutes), formalin 10% (10 minutes), chlorhexidine gluconate 5% (10 minutes), silver nitrate (5 minutes) to prevent recurrence.14 The surgical procedure may be combined with 3 cycles of tablet albendazole 400 mg twice a day for 28 days (with a periodic gap of 14 days) to prevent recurrence. The patient must be kept under long term clinical evaluation after surgery, to check for recurrence.

This patient had not been operated for hydatid disease previously and investigations did not reveal any hydatid cyst in brain, liver, lung or spleen. So this patient was diagnosed, having primary hydatid disease of musculoskeletal system.

Though intramuscular hydatid cysts are reported in literature as rare findings, any description of hydatid cyst in intercostal muscles could not be located in the literature.

Funding: None

Conflict of interest: None declared

Ethical approval: Not required

REFERENCES

  1. 1. Mirdha BR, Biswas A. Echinocossis: Presenting as palpable lumps of breast. Indian J Chest Dis Allied Sci. 2001;43:241.
  2. 2. Goel MC, Aggarwal MR, Misra A. Percutaneous drainage of renal hydatid cyst: early results and follow-up. Br J Urol. 1995;75:724-8.
  3. 3. Altinors N, Senveli E, Donmez T, Bavbek M, Kars Z, Sanli M. Management of problematic intracranial hydatid cysts. Infection. 1995;23:283-7.
  4. 4. Brown RA, Millar AIW, Steiner Z, Krige JEJ, Burkimsher D, Cywes S. Hydatid cust of pancreas: A case report in a child. Eur J Pediatr Surg. 1995;5:121-4.
  5. 5. Kir A, Baran E. Simultaneous operation for hydatid cyst of right lung and liver. Thorac Cardiovasc Surgeon. 1995;43:62-4.
  6. 6. Guntz M, Coppo B, Lorimier G, Cronier P. Hydatid cyst of the liver appearing late (10-22 years) after surgical treatment of pulmonary hydatidosis. Physiopathologic problems. J Chir Paris. 1990;127:375-81.
  7. 7. Eshy SAA. Some rare presentations of hydatid cyst. JR Coll Surg Edinb. 1998;43:347-52.
  8. 8. Milanese A, Camana GP, Carbone P. Echinococcus cyst in the pelvic cavity: Presentation of case. Minerva Urol Nephrol. 1991;43:301-3.
  9. 9. Abdel-khaliq RA, Othman Y. Hydtid cyst of pectoralis major muscle. A case report and note on surgical management of muscle echinococossis. Acta Chir Scand. 1986;152:469-71.
  10. 10. Cangiotti L, Muiesan P, Begni A, de Cesare V, Pouchè A, Giulini SM, et al. Unusual localization of hydatid disease: An 18-year experience. G Chir. 1994;15:83-6.
  11. 11. García-Alvarez F, Torcal J, Slinas JC, Navarro A, García-Alvarez I, Navarro-Zorraquino M, et al. Musculoskeletal hydatid disease: A report of 13 cases. Acta Orthop Scand. 2002;73:227-31.
  12. 12. Tatari H, Baran O, Sanlidağ T, Göre O, Ak D, Manisali M, et al. Primary intramuscular hydatidosis of supraspinatus muscle. Arch Orthop Trauma Surg. 2001;121:93-4.
  13. 13. Kacheriwala SM, Mehta KD, Pillai B, Jain Y. A rare presentation of primary hydatid cyst. Indian J Surg. 2004;66(1):47-9.
  14. 14. Fischer JE. Fischer’s Mastery of Surgery. 6th ed. Wolters Kluwer; Lippincott Williams and Wilkins; 2012: 1189-1211.