2.Botryomycosis secondary to Staphylococcus simulans masquerading as mycetoma in a 46-year-old Filipino female.
Ysabel Regina H. Ortiz ; Maria Christina Filomena R. Batac
Acta Medica Philippina 2024;58(17):64-68
Botryomycosis is a rare pyogenic disease that presents with chronic suppurative and granulomatous skin lesions, commonly caused by Staphylococcus aureus. We report a case of botryomycosis presenting similarly to mycetoma, secondary to the emerging cutaneous pathogen Staphylococcus simulans. A 46-year-old female who previously worked in a wet market presented with a 13-year history of suppurative papules on a gradually enlarging right foot, and pain on ambulation. She had no systemic symptoms or co-morbidities, and does not recall preceding trauma. Physical examination showed brawny edema of the right foot with multiple sinus tracts draining purulent discharge. The clinical diagnosis at presentation was mycetoma. Magnetic resonance imaging showed a soft tissue mass involving the right foot and ankle with osseous destruction. Biopsy revealed suppurative granulomatous dermatitis; staining with Grocott methenamine silver did not highlight fungal elements. Potassium hydroxide mount of the purulent discharge did not show grains or hyphal elements. Tissue cultures showed growth of co-trimoxazole-susceptible Staphylococcus simulans. The patient was managed as a case of botryomycosis and treated with co-trimoxazole for 12 months. There was a significant decrease in right foot circumference along with scarring and resolution of associated pain. Repeat biopsy showed no evidence of infection. This is the first reported case of botryomycosis in the Philippines as well as the first report citing Staphyloccocus simulans as a causative agent. Botryomycosis is an important differential in patients clinically presenting as mycetoma. Animal pathogens may need to be considered as etiologic agents in at-risk patients with chronic subcutaneous infections.
Human ; Female ; Middle Aged: 45-64 Yrs Old ; Mycetoma
6.Conjunction of a Fungus Ball and a Pulmonary Tumourlet in a Bronchiectatic Cavity.
Serkan YAZGAN ; Soner GÜRSOY ; Figen TÜRK ; Zekiye Aydoğdu DINÇ
The Korean Journal of Thoracic and Cardiovascular Surgery 2018;51(2):138-141
Herein, we describe the case of a 67-year-old female patient who presented with cough and haemoptysis. Chest computed tomography revealed destruction of the left lower lobe and multiple fungus balls in a bronchiectatic cavity. A left lower lobectomy was performed via thoracotomy. Histopathological examination of the lung showed a concomitant aspergilloma and multiple tumourlets in the large bronchiectatic cavity. Pulmonary intracavitary aspergilloma and concomitant tumourlets are quite rare. Our report presents this interesting case that manifested with haemoptysis.
Aged
;
Bronchiectasis
;
Cough
;
Female
;
Fungi*
;
Hemoptysis
;
Humans
;
Lung
;
Mycetoma
;
Pulmonary Aspergillosis
;
Thoracotomy
;
Thorax
7.Primary Cutaneous Nocardiosis Caused by Nocardia niigatensis.
Dong Uk CHEON ; Yang Soon LEE ; Joo Yeon KO ; Young Suck RO ; Jeong Eun KIM
Korean Journal of Dermatology 2018;56(5):347-349
No abstract available.
Nocardia Infections*
;
Nocardia*
8.Severe Sepsis and Empyema Caused by Nocardia.
Ha Youn LEE ; Young Sik PARK ; Sang Min LEE ; Jinwoo LEE
Korean Journal of Medicine 2018;93(3):296-299
Pulmonary nocardiosis is a rare opportunistic infection that commonly affects immunocompromised hosts, such as patients with organ transplants, acquired immunodeficiency syndrome, or prolonged immunosuppression. Recently, we encountered a case of pulmonary nocardiosis with empyema that progressed to severe sepsis. The patient was treated in the intensive care unit. Thereafter, medical thoracoscopy was performed to improve drainage of the pleural fluid. Nocardia was identified in the culture of the pleural fluid.
Acquired Immunodeficiency Syndrome
;
Drainage
;
Empyema*
;
Humans
;
Immunocompromised Host
;
Immunosuppression
;
Intensive Care Units
;
Nocardia Infections
;
Nocardia*
;
Opportunistic Infections
;
Sepsis*
;
Thoracoscopy
;
Transplants
9.Mistaken identity: Eumycetoma masquerading as Squamous cell carcinoma
Catherina Jessica Sutantoyo ; Johannes F. Dayrit ; Ma. Teresita G. Gabriel ; Glen Purnomo ; Reynaldo L. Ugalde
Journal of the Philippine Dermatological Society 2018;27(1):81-83
We report a case of eumycetoma in a Filipino patient who presented with a solitary reddish brown, moist, multinodular tumor on the
dorsum of the left foot of 2 years duration. Biopsy with Periodic acid Schiff (PAS) & Gomori methenamine silver (GMS) staining, fungal
culture, ultrasound and X-ray of the foot were done in our institution which confirmed the diagnosis of eumycetoma. The patient was
successfully treated with itraconazole 400/day for 3 months, followed by 200mg/day for the succeeding 9 months, leading to complete
resolution of the lesion leaving an atrophic hypopigmented scar. A high index of suspicion supported by diagnostic tests aided in the
early detection of the disease which also resulted to complete resolution of the disease.
Mycetoma
;
Mycoses
;
Itraconazole
10.Primary Cutaneous Nocardiosis Caused by Nocardia takedensis.
Taek Geun LEE ; Woo Jung JIN ; Woo Seok JEONG ; Seung Hyun MOON ; Tae Gwang KWON ; Sook Kyung LEE ; Hye Sook KANG ; Hyun HWANGBO
Annals of Dermatology 2017;29(4):471-475
Nocardia species are aerobic, gram-positive, filamentous, partially acid-fast actinomycetes which are found worldwide in soil and decaying organic plant matter. When they infect human beings, they generally enter through the respiratory tract and then disseminate systemically. Rarely has a primary infection occurred as the result of direct inoculation. Isolation of Nocardia from clinical specimens and identification of species are difficult. But, with the introduction of new genetic technologies, reports of novel species of Nocardia have increased. We describe a case of cutaneous nocardiosis caused by Nocardia takedensis in an 87-year-old woman who was diagnosed by bacterial culture and 16S ribosomal RNA sequencing. N. takedensis has been described as a new species. This report describes the first clinical isolate of N. takedensis from a skin specimen in Korea.
Actinobacteria
;
Aged, 80 and over
;
Female
;
Humans
;
Korea
;
Nocardia Infections*
;
Nocardia*
;
Plants
;
Respiratory System
;
RNA, Ribosomal, 16S
;
Skin
;
Soil


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