Highlights
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Primary chest wall hydatid cyst is an extremely rare disease.
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It occurs in endemic area and usually diagnosed intraoperatively.
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In this report, we reported a case of primary chest wall Hydatid cyst with review of literature.
Keywords: Hydatid cyst, Pregnancy, Albendazole
Abstract
Introduction
Hydatid cyst is a parasitic disease caused by Echinococci. The most commonly affected organ is liver, followed by lungs. Hydatid disease of the chest wall is extremely rare. The aim of this study is to report a case of chest wall Hydatid cyst with literature review. A 20-year-old pregnant lady presented with left hypochondrial and lower chest painful swelling. There was 10 × 15 centimeters, tender mass with features suggestive of abscess. The patient refused every sort of radiological examination. Under general anesthesia, oblique incision was done, on opening, clear fluid came out, with deep incision pus-like fluid and many daughter cysts drained. Complete evacuation of the cyst was done with closure of the residual cavity. The patient refused chemoprophylaxis because of her pregnancy.
Conclusion
primary chest wall Hydatid cyst is a very rare disease in endemic areas. Mass and pain are the most common presentation. Excision under general anesthesia is main modality of treatment.
1. Introduction
Hydatid cyst (HC) is a serious, endemic, parasitic disease caused by Echinococcus cestode [1]. It is endemic in sheep-farming areas of Greece, Middle East, Australasia, Sub-Saharan Africa, parts of America, and India [2]. Dog is the primary host while intermediate hosts are horse, cattle and sheep. Although humans do not share the life cycle, they may be affected accidentally. Infection is occurring either by direct contact with dog or contaminated food and fluid by eggs [2]. The most commonly affected organ is liver (52%–77%), followed by lungs (10%–40%) [3]. Rarely, it affects diaphragm, vertebrae, abdominal wall and skeletal muscles [4], [5], [6]. Hydatid disease of the chest wall is extremely rare. It might form due to either rupture of lung HC into the pleural space [3]. Primary chest wall HC is even rarer with only eight reported cases in literature [1], [2], [3], [7], [8], [9], [10], [11].
Although it is well known that HC may affect any area of the body, reporting of cases occurring in rare organs is necessary because both presentation and clinical course of the disease differ. The aim of this study is to report a case of chest wall HC occurring in a 20-year-old pregnant lady in line with SCARE guideline with literature review [12].
1.1. Patient information
A 20-year-old, housewife, one missed period pregnant lady presented with left hypochondrial and lower chest wall painful swelling. She had this swelling for 5 years but of smaller size and no pain. In last few days, sudden increase in size occurred and became painful. They live in rural area with history of contact with domestic animals including dogs and sheeps. Her parents have been operated on for liver HC. Drug history was negative.
1.2. Clinical findings
There was 10 × 15 centimeters, tender mass with induration and overlying skin erythema, fixed to underlying chest wall.
1.3. Diagnostic assessment
The patient refused every sort of radiological examination including ultrasound because of her pregnancy. Complete blood counts and virology tests were normal.
1.4. Therapeutic intervention
Under general anesthesia, in supine position, the area was isolated by iodinized pack. Oblique incision was done, on opening, clear fluid came out, with deep incision pus-like fluid and many daughter cysts drained (Fig. 1). Complete evacuation of the cyst was done with closure of the residual cavity. Drain was put. The wound closed. The procedure was performed by the second author, supervised by first author and assisted by the last author.
Fig. 1.
(A) Lamina of Hydatid cyst. (B) Multiple daughter cysts.
1.5. Follow-up and outcomes
She was advised to terminate her pregnancy and receive Antihelminthic medication but she refused. The patient was sent home after overnight admission with oral antibiotic and analgesic. Three months later, the scar was clean and healthy, the baby was viable. Later she was los from follow up.
2. Discussion
HC which is caused by Echinococcus granulosus, transmits to humans either by direct contact with dogs or by eating contaminated food [2], [3], [7]. The current case reported contact with domestic animals. There is no age limit for HC affection. Admir et al. reported chest wall HC in a 9 year old male presenting with mass and chest pain for one month duration, for which benign lesion was the provisional diagnosis, while Avci et al. reported a 72-year-old female presenting with pain [1], [3]. Chest wall HC is a slow growing mass and it may be present for a long time before developing complications [9]. This lady presented with chest wall swelling for 5 years, developing hypochondrial and lower chest pain just few days before operation. According to the literatures, there are two mechanisms of primary chest wall HC. The first one is systemic spread of the embryo from the duodenal wall into the portal system or into the perigastric lymphatics which subsequently drain to the right lymphatic and the thoracic ducts and the second one local extension from the surrounding thoracic organ with disappearance of the primary source [2]. Expectoration and haemoptysis might be seen if there is involvement of pulmonary parenchyma but the current case had not have respiratory symptoms [2]. The diagnosis of HC is radiological. Indirect hemaglutination test, complimentary fixation test and dermal test may aid in diagnosis but they are neither sensitive nor specific [1], [2], [4], [8]. Diagnosis of chest wall HC is challenging [8]. Argaw et al. perfomed fine needle aspiration for infraclavicular chest wall cystic lesion which showed features of lymphangioma, later exploration confirmed diagnosis of chest wall HC [2]. Alloubi and his associates managed a case of chest wall HC with provisional diagnosis of bronchogenic carcinoma invading chest wall with destruction of ribs [8]. The current case denied any sort of radiological examinations because of the pregnancy and other hematological tests were not performed as the provisional diagnosis was chest wall abscess and HC was not put in differential diagnosis. The latter was the motive for reporting this case and it is the main important learning point. Among cases of extrapulmonary thoracic HC, 2.3% reported rib destruction and full thickness chest wall involvement [9], [11]. In this case, the mass was subcutaneous, partially involving muscular layers while the ribs were free from the disease. Accr et al. suggested that combined surgery and chemotherapy (Albendazole) for pre and post-operative prophylaxis provides a good outcome [2]. This case did not receive pre-operative antihelmintics and post-operative chemoprophylaxis was refused because of conception. Table 1 shows brief literature review regarding the reported cases of chest wall HC.
Table 1.
literature review of the all eight reported cases of chest wall Hydatid cyst.
| Author/ references | Age(years)/Sex | Presentation | Duration | Provisional diagnosis |
|---|---|---|---|---|
| 1/Demir et al | 9/male | Chest pain | 1 month | Benign lesion |
| 2/Argaw et al | 36/female | Pain, swelling | 2 years | Lymphangioma |
| 3/Avci et al | 72/female | Chest pain | Not mentioned | posttraumatic haematoma |
| 7/Tulay et al | 48/male | swelling | 5 months | Not mentioned |
| 8/Alloubi et al | 57/male | Chest pain | 3 months | Malignant tumor |
| 9/Karapolat et al | 69/female | Abdominal pain | 4 years | Malignant tumor |
| 10/Sarkar et al | 58/female | Lump | 3 years | Hydatid cyst |
| 11/Goyal et al | 30/female | Pain, swelling | Not mentioned | Not mentioned |
In conclusion, primary chest wall HC is a very rare disease in endemic areas. Mass and pain are the most common presentation. Excision under general anesthesia is main modality of treatment.
Patient perspective
The patient was satisfied with the outcome of the operation.
Conflicts of interest
There is no conflict to be declared.
Funding
No source to be stated.
Ethical approval
Approval has been taken from Kscien organization.
Consent
The patient gave consent for publication of the report.
Author contribution
Abdulwahid M. Salih, Dilshad M. Ahmed and Hanna M. Ali2: supervised and performed the operation and follow up.
Fahmi H. Kakamad, Hunar A.H and Rawand A. Essa: writing the manuscript and follow up.
Guarantor
Fahmi Hussein kakamad.
References
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