Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Edward J. Wills"'
Autor:
Richard A. Scolyer, Edward J. Wills, Wendy A Cooper, Jane Hollingsworth, C. Soon Lee, Katherine D. Nicoll, Vallapan Thiruvilangam
Publikováno v:
Pathology. 43:67-70
Publikováno v:
Burns. 36:49-56
Purpose: Following a burn, the wound may become colonized and septic complications may ensue. Many organisms, commonly isolated from burn wounds produce biofilms, which are defined as a collection of organisms on a surface surrounded by a matrix. Bio
Publikováno v:
Journal of Neuro-Oncology. 84:91-98
We report a case of a 2 year-old boy who initially presented with macrocephaly and severe global developmental delay. Imaging revealed a large left temporo-parietal mass that was lobulated, calcified, focally enhancing and partially cystic. A second
Publikováno v:
Muscle & Nerve. 35:536-539
Polyglucosan body disease (PBD) is a slowly progressive adult-onset glycogen storage disorder that typically affects upper and lower neurons. Myopathy, as a complication of PBD has been reported rarely and clinically manifests as chronic limb-girdle
Autor:
Danielle E. Dye, Clive Harper, Adam Maxwell, Meena Shingde, Kathryn N. North, Nigel G. Laing, Penelope J. Spring, Edward J. Wills
Publikováno v:
Neuromuscular Disorders. 16:882-886
Myosin storage myopathy/hyaline body myopathy is a rare congenital myopathy, with less than 30 cases reported in the literature. It is characterised by the presence of subsarcolemmal hyaline bodies in type 1 muscle fibres and predominantly proximal m
Publikováno v:
Pathology International. 56:89-94
Myxoid variant of adrenocortical carcinomas (ACC) are rare, there being only 11 cases in the literature to date. Reported herein are the findings of a case, which in contrast to all previously reported myxoid ACC, was devoid of typical non-myxoid are
Publikováno v:
Ultrastructural Pathology. 27:79-86
During the routine examination of a segment of colon resected for adenocarcinoma, a diffuse proliferation of mucosal tactile corpuscle-like bodies was identified. The bodies showed a lamellar structure by light microscopy and were S-100 positive. Ele
Publikováno v:
Australasian Journal of Dermatology. 53:278-280
Ehlers-Danlos syndrome (EDS) is a group of inherited connective tissue disorders. The clinical manifestations are heterogeneous and usually generalised. We present a case of mosaic EDS, an extremely rare variant. Our patient presented with a single l
Publikováno v:
Pathology. 33:101-107
Summary Hyalinising spindle cell tumour with giant rosettes (HSCTGR) is an uncommon, recently described low-grade sarcoma which shares many histological features with low-grade fibromyxoid sarcoma (LGFMS). We report a case of HSCTGR occurring in the
Publikováno v:
Ultrastructural Pathology. 25:275-279
Microvillous inclusion disease is a rare lethal disorder characterized by intractable, severe, watery diarrhea beginning in early infancy. The underlying defect is thought to be an autosomal recessive genetic abnormality resulting in defective brush-