1.
Clin Exp Dermatol
; 47(8): 1588-1590, 2022 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35426452
RESUMO
We describe the successful use of rituximab for the treatment of IgA nephropathy in a patient with recessive dystrophic epidermolysis bullosa. To our knowledge, this is the first reported case in the literature.
Assuntos
Antineoplásicos , Epidermólise Bolhosa Distrófica , Epidermólise Bolhosa , Glomerulonefrite por IGA , Anticorpos Monoclonais , Epidermólise Bolhosa Distrófica/complicações , Epidermólise Bolhosa Distrófica/tratamento farmacológico , Glomerulonefrite por IGA/complicações , Glomerulonefrite por IGA/tratamento farmacológico , Humanos , Rituximab/uso terapêutico
2.
J Cutan Pathol
; 47(7): 628-632, 2020 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32020668
RESUMO
We report a case of a 76-year-old man presenting with a 12-month history of a solitary lesion on his scalp. The histopathology was consistent with a grade 2/3 osteosarcoma extending to the subcutis. Full-body imaging excluded any involvement of the underlying bony tissue or solid organ malignancy, thus a diagnosis of primary cutaneous osteosarcoma (PCO) was made. Given the exceedingly rare nature of PCO, we discuss the clinico-pathological features of this case and those previously reported in the literature.