Unilateral case of multiple minute digitate hyperkeratosis

2019 ◽  
Vol 46 (6) ◽  
pp. e210-e211
Author(s):  
Satoko Okochi ◽  
Michihiro Kono ◽  
Hiromichi Takama ◽  
Takuya Takeichi ◽  
Yoshinao Muro ◽  
...  
Keyword(s):  
2021 ◽  
pp. 378-385
Author(s):  
Hitoshi Sugimoto ◽  
Goshi Oda ◽  
Minato Yokoyama ◽  
Kumiko Hayashi ◽  
Maho Yoshino ◽  
...  

Breast cancer metastasizes mainly to organs such as bone, lung, and liver, whereas metastases to the peritoneum and urinary tract are rare. Metastasis to the peritoneum or urinary tract may result in renal dysfunction, infection, and painful hydronephrosis. In our hospital, 1,409 breast cancer surgeries were performed between January 2004 and December 2015, and 7 cases of hydronephrosis associated with recurrence were observed. The median age of patients was 69 years (57–79 years). The median time from surgery to diagnosis of hydronephrosis was 47 months (20–70 months). Histology was invasive ductal carcinoma (IDC) in 6 cases and invasive lobular carcinoma (ILC) in 1 case. There were 6 bilateral cases and 1 unilateral case of hydronephrosis. The causes were retroperitoneal metastasis in 5 cases and lymph node metastasis in 2 cases. The hydronephrosis was untreated in 2 cases, and treated with a ureteral stent in 2 cases, nephrostomy in 1 case, and nephrostomy due to ureteral stent failure in 2 cases. The median survival from the onset of hydronephrosis was 12 months (3–57 months). Although the probability of hydronephrosis in breast cancer recurrence was not high, care must be taken to avoid renal dysfunction, infection, or pain, which may require treatment.


2019 ◽  
Vol 63 (5) ◽  
pp. 374-381 ◽  
Author(s):  
Yoichi Sakurada ◽  
Atsushi Sugiyama ◽  
Wataru Kikushima ◽  
Seigo Yoneyama ◽  
Naohiko Tanabe ◽  
...  

1991 ◽  
Vol 11 (2) ◽  
pp. 303-309 ◽  
Author(s):  
Gordan M. Vujanić
Keyword(s):  

Cornea ◽  
2010 ◽  
Vol 29 (12) ◽  
pp. 1462-1464 ◽  
Author(s):  
Athena Roufas ◽  
Peter Kim ◽  
Dianne Reeves ◽  
Gerard Sutton

2017 ◽  
Vol 102 (5) ◽  
pp. 622-624 ◽  
Author(s):  
Anne-Marie Hinds ◽  
Abigail Fahim ◽  
Anthony T Moore ◽  
Sui Chien Wong ◽  
Michel Michaelides

Background/AimsA subset of patients with X linked retinoschisis (XLRS) have bullous schisis cavities in the peripheral retina. This study describes the characteristics and prognosis of the bullous form of XLRS.MethodsA retrospective case series was performed of nine patients with molecularly proven bullous XLRS seen at a single tertiary centre.ResultsAll cases of bullous peripheral schisis were bilateral, with one unilateral case at presentation which developed into bilateral bullous schisis over time. The mean age of onset was 1.9 years (range: 1 month–7 years, SD: 2.1 years) and at clinical diagnosis was 5.9 years (range: 1 month–27 years, SD: 9.0 years). Mean follow-up was 11 years (range: 6 months–36 years, SD: 10.8 years). Strabismus was the most common presentation (n=7). Other presenting complaints included decreased vision, floaters and an irregularly shaped pupil. The most frequently associated ocular features were strabismus (100%), vitreous haemorrhage (4/18 eyes, 22%), nystagmus (2/9, 22%) and persistent fetal vasculature (1/18, 6%). Localised tractional detachment was seen in 2/18 (11%) eyes, total detachment that underwent surgical repair in 1/18 (6%) and pigmented demarcation lines in a further 22% of the eyes. There was one eye with exudative retinal detachment.ConclusionIn XLRS, bullous schisis may be congenital or develop soon after birth and most commonly presents with strabismus. Cases may be complicated by some form of retinal detachment, which may be tractional or a Coats-like exudative detachment.


1996 ◽  
Vol 50 (2) ◽  
pp. 85-88 ◽  
Author(s):  
MASATO FUKUDA ◽  
AKINOBU HATA ◽  
SHIN-ICHI NIWA ◽  
KEN-ICHI HIRAMATSU ◽  
MASAFUMI YOKOKOJI ◽  
...  

2014 ◽  
Vol 15 (2) ◽  
pp. 127-130
Author(s):  
Erkan Unsal ◽  
Yeliz Acar ◽  
Kadir Eltutar

2003 ◽  
Vol 38 (2) ◽  
pp. 259-261 ◽  
Author(s):  
Giovanni Cecchetto ◽  
Rita Alaggio ◽  
Giovanni Scarzello ◽  
Patrizia Dall'Igna ◽  
Ascanio Martino ◽  
...  
Keyword(s):  

2016 ◽  
Vol 33 (01) ◽  
pp. 029-031
Author(s):  
B. Ghosh ◽  
S. Yadav ◽  
V. Budhiraja ◽  
P. Dass ◽  
R. Rastogi ◽  
...  

Abstract Introduction: Variation of the ulnar artery in the upper limb is uncommon. The existence of such a variant is of particular clinical significance, as these arteries are more susceptible to trauma, and can be easily confused with superficial veins during medical and surgical procedures, potentially leading to iatrogenic distal limb ischemia. Case report: During routine dissection we observed a unilateral case of superficial ulnar artery in a 60-year-old male cadaver. It originated from the left brachial artery in the middle of the arm, near to insertion of coracobrachialis muscle. From its origin, it passed downwards in the medial part of arm behind the median nerve and forearm in a supericial plane compared to normal ulnar artery. In the hand, the supericial ulnar artery anastomosed with the palmar branch of the radial artery, creating the supericial palmar arch. Brachial artery divided into the radial and common interosseous arteries in the cubital fossa. The normal ulnar artery was absent. The existence of superficial ulnar artery is undeniably of interest to the clinicians as well as to the anatomists.


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