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Pulmonary Mucormycosis and hydatid cyst: A case report
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AbstractMucormycosis is a group of life‐threatening diseases caused by a fungus of the Mucoraceae family and has a higher mortality rate compared with other known fungal infections. Hydatid cyst, caused by Echinococcus, is a crucial health concern in endemic areas and the disease is characterized by slow‐growing cysts in the liver, lungs, or other organs. In this report, a woman with coexistence of hydatid cyst and Mucormycosis is introduced. The patient was a 52‐year‐old woman with approximately 6 years' history of uncontrolled diabetes mellitus and hypothyroidism, who presented with cough, sputum, and dyspnea 2 months ago. On the initial auscultation of the lungs, there was a decreased sound at the base of the left lung, and she had a fever. In blood tests, she had a high titer of erythrocyte sedimentation rate and 3+ C‐Reactive Protein. The symptoms in favor of hydatid cyst were observed in lung computed tomography and in pleural needle biopsy, hydatid cyst was confirmed. With this indication, she underwent wedge resection, and resection of the left lower lung cyst. Two samples are taken from the cyst side and the pathology report was consistent with Mucormycosis (wide filaments with a 90‐degree angle). The patient was immediately treated with liposomal amphotericin for 4 weeks. The Lung CT scan was performed before and after treatment. Albendazole was treated to treat hydatid cyst. After discharge, the treatment of the patient continued with oral Posaconazole, and after the treatment finalization, the general condition of the patient was good, and she did not have any complaints. In pulmonary diseases that do not respond significantly to surgical treatment (such as hydatid cyst), fungal disease (mucor) must be considered simultaneously. Mucormycosis is more prevalent in patients with uncontrolled diabetes, and it is necessary to be considered if these patients were infected with pneumonia and their symptoms did not improve with usual treatments.
Title: Pulmonary Mucormycosis and hydatid cyst: A case report
Description:
AbstractMucormycosis is a group of life‐threatening diseases caused by a fungus of the Mucoraceae family and has a higher mortality rate compared with other known fungal infections.
Hydatid cyst, caused by Echinococcus, is a crucial health concern in endemic areas and the disease is characterized by slow‐growing cysts in the liver, lungs, or other organs.
In this report, a woman with coexistence of hydatid cyst and Mucormycosis is introduced.
The patient was a 52‐year‐old woman with approximately 6 years' history of uncontrolled diabetes mellitus and hypothyroidism, who presented with cough, sputum, and dyspnea 2 months ago.
On the initial auscultation of the lungs, there was a decreased sound at the base of the left lung, and she had a fever.
In blood tests, she had a high titer of erythrocyte sedimentation rate and 3+ C‐Reactive Protein.
The symptoms in favor of hydatid cyst were observed in lung computed tomography and in pleural needle biopsy, hydatid cyst was confirmed.
With this indication, she underwent wedge resection, and resection of the left lower lung cyst.
Two samples are taken from the cyst side and the pathology report was consistent with Mucormycosis (wide filaments with a 90‐degree angle).
The patient was immediately treated with liposomal amphotericin for 4 weeks.
The Lung CT scan was performed before and after treatment.
Albendazole was treated to treat hydatid cyst.
After discharge, the treatment of the patient continued with oral Posaconazole, and after the treatment finalization, the general condition of the patient was good, and she did not have any complaints.
In pulmonary diseases that do not respond significantly to surgical treatment (such as hydatid cyst), fungal disease (mucor) must be considered simultaneously.
Mucormycosis is more prevalent in patients with uncontrolled diabetes, and it is necessary to be considered if these patients were infected with pneumonia and their symptoms did not improve with usual treatments.
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