EAS Publisher | A Rare Case Report on Mediastinal Lipomatosis

A Rare Case Report on Mediastinal Lipomatosis

DOI : https://doi.org/10.36349/easjmb.2020.v03i11.001

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Abstract: Mediastinal lipomatosis is a rare condition characterised by a large amount of mature adipose tissue in the mediastinum. For 6 months, a case of dyspnea, breathlessness and cough, originally misdiagnosed as a case of right lower lobe pneumonia, was found to have mediastinal lipomatosis dependent on CT on further examination and validated with HPE association after excision. This case of ML occurred in the absence of steroid use, diabetes, the condition of Cushing. This case provides a major differential diagnosis of a patient with dyspnea. Potentially, this is one of the few instances of ML.

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Lecturer, Dept. of Pharmacology and Therapeutics, Shaheed Monsur Ali Medical College & Hospital, Uttara, Dhaka-1230, Bangladesh

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