Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Carolyn J Shiau"'
Publikováno v:
SAGE Open Medical Case Reports, Vol 12 (2024)
Syphilis is a sexually transmitted infection that is undergoing a resurgence in Canada and around the world. If not diagnosed correctly, syphilis can progress to its secondary and tertiary stages, affecting numerous organ systems. We present a case o
Externí odkaz:
https://doaj.org/article/b823423d665c48abb95ae53e7d2acb48
Publikováno v:
SAGE Open Medical Case Reports, Vol 10 (2022)
Bullous pemphigoid is an acquired autoimmune blistering dermatosis that is commonly associated with high morbidity and mortality. New-onset bullous pemphigoid following vaccinations has rarely been reported in the literature. We report two cases of n
Externí odkaz:
https://doaj.org/article/e542043f0359432b88c12319e6d90cd7
Publikováno v:
SAGE Open Medical Case Reports, Vol 9 (2021)
Background: Sinus histiocytosis with massive lymphadenopathy, also known as Rosai–Dorfman disease, is a rare proliferation of non-Langerhans histiocytes. Cutaneous Rosai–Dorfman disease is a rare subtype of Rosai–Dorfman disease limited to the
Externí odkaz:
https://doaj.org/article/213919e14a7a40dca9f918aeb9fc97e7
Publikováno v:
Journal of Clinical Pathology. 72:438-442
Benign spindle cell lesions of the breast include neoplastic and reactive entities that are diagnostically challenging given their rarity and similar histomorphology. Accurate diagnosis on percutaneous core biopsy within this category is essential as
Publikováno v:
The American Journal of the Medical Sciences. 354:486-492
Persistent eosinophilia can cause cardiac tissue damage, typically in the form of eosinophilic myocarditis, whether the underlying cause is reactive, a clonal myeloid disorder, or idiopathic hypereosinophilic syndrome (HES). Eosinophilic myocarditis
Publikováno v:
SAGE Open Medical Case Reports
SAGE Open Medical Case Reports, Vol 9 (2021)
SAGE Open Medical Case Reports, Vol 9 (2021)
Background: Sinus histiocytosis with massive lymphadenopathy, also known as Rosai–Dorfman disease, is a rare proliferation of non-Langerhans histiocytes. Cutaneous Rosai–Dorfman disease is a rare subtype of Rosai–Dorfman disease limited to the
Publikováno v:
Journal of Clinical Pathology. 68:954-962
The diagnosis of panniculitis is a relatively rare occurrence for many practising pathologists. The smaller subset of lymphocyte-predominant panniculitis is further complicated by the diagnostic consideration of T cell lymphoma involving the subcutan
Publikováno v:
Journal of cutaneous medicine and surgery. 22(1)
Background: CD34-positive plaque-like dermal fibroma (PDF) is a poorly characterised benign dermal neoplasm that has a wide differential diagnosis. It can be mistaken for other entities on superficial biopsy and be overtreated, leading to unnecessary
Autor:
Jenna Sykes, Scott L. Boerner, Jesse Paul Babwah, Ming-Sound Tsao, Natasha B. Leighl, Cuihong Wei, Gilda da Cunha Santos, David M. Hwang, Suzanne Kamel-Reid, Carolyn J. Shiau, William R. Geddie
Publikováno v:
Journal of Thoracic Oncology. 9:947-956
Introduction: Epidermal growth factor receptor ( EGFR ) mutation testing has become critical in the treatment of patients with advanced non–small-cell lung cancer. This study involves a large cohort and epidemiologically unselected series of EGFR m
Publikováno v:
Expert Review of Dermatology. 8:195-214
The diagnosis of lentigo maligna (LM) is often challenging for both clinicians and pathologists. LM is widely regarded as a form of melanoma in situ occurring in severely sun-damaged skin with characteristic clinical and pathologic features. However,