scholarly journals A rare disorder in an orphan disease: Kikuchi-Fujimoto disease in a young-adult patient with sickle cell anemia

2014 ◽  
Vol 89 (12) ◽  
pp. 1151-1152 ◽  
Author(s):  
Elisa Vencato ◽  
Riccardo Manfredi ◽  
Alberto Zamò ◽  
Marco Chilosi ◽  
Serena Beccari ◽  
...  
2005 ◽  
Vol 100 (12) ◽  
pp. 2818-2821 ◽  
Author(s):  
Simona Sada ◽  
Luigi Benini ◽  
Chiara Pavan ◽  
Maria Novella Favalli ◽  
Giancarlo Mansueto ◽  
...  

2001 ◽  
Vol 90 (6) ◽  
pp. 1070-1072
Author(s):  
Emi Tajima ◽  
Hidetsugu Mihara ◽  
Motohiro Wakabayashi ◽  
Masaya Watarai ◽  
Kazutaka Sugamura ◽  
...  

2018 ◽  
Vol 66 (1) ◽  
pp. e27491 ◽  
Author(s):  
Shree Bose ◽  
Joanna Robles ◽  
Chad M. McCall ◽  
Anand S. Lagoo ◽  
Daniel S. Wechsler ◽  
...  

1986 ◽  
Vol 8 (6) ◽  
pp. 165-167
Author(s):  
James E. Rasmussen

Pearly penile papules are common but not commonly seen in a physician's office. These multiple, white, coronal papules are rarely, if ever, the source of a disease but may cause the adolescent and young adult patient some surprise when they are first noticed. "Discovery" may occur after careful self-examination following suspected contact with venereal disease, sexual exposure, masturbation, or other situations that may be associated with anxiety. Frequently, the patient believes that the lesions originated "overnight"; this is never the case and usually represents inaccurate observation. Lesions of pearly penile papules are characteristic in morphology and locale. They occur exclusively in postpubertal patients. Neinstein and Goldenring1 found pearly penile papules in 23 of 151 (15.2%) boys and men ranging from 11 to 22 years of age. Lesions were not noted in patients less than 14 years old or with a sexual maturity rating less than a Tanner 3. Glicksman and Freeman2 examined 229 men and found these lesions in 45 (20%). There does not appear to be any racial tendency, and whereas one series found a greater percentage in uncircumcised patients,2 a second could not substantiate this possibility.1 Although no surveys have been done in prepubertal patients, it is my clinical impression that these lesions do not occur in this age group.


Blood ◽  
1958 ◽  
Vol 13 (6) ◽  
pp. 569-581 ◽  
Author(s):  
C. C. SPRAGUE ◽  
J. C. S. PATERSON

Abstract The survival of sickle cell anemia and sickle-cell/Hb-C erythrocytes was determined by the radioactive chromium method, both in their parent circulations and in the circulations of compatible normal recipients. In sickle cell anemia patients with splenomegaly the average erythrocyte survival time (T½) was found to be 3.7 days. After splenectomy T½ increased to an average of 11.4 days. In sickle cell anemia patients without splenomegaly the average T½ was found to be 10 days. In five instances an average T½ of 9.2 days was found, whereas the average T½ for the same cells in the circulations of normal recipients was 4.4 days. In sickle-cell/Hb-C disease the average T½ was 15.7 days. Following splenectomy in two patients, T½ was unchanged in one and increased in the second. T½ was shortened in two of three instances when these cells were transfused into normal recipients, but the data are insufficient to permit conclusions to be drawn. The role of the spleen in hemolysis is discussed briefly and it is concluded that the hemolytic process in sickle cell anemia is accelerated in the presence of a spleen. This finding is compatible with the diminution in the severity of sickle cell anemia frequently recognized in the adult patient whose spleen has atrophied, and in the child following splenectomy. The validity of the chromate-tagging method for determining erythrocyte survival is discussed. Splenectomy was performed in children in whom the erythrocyte survival was shortened (T½ less than 6 days).


Surgery Today ◽  
2007 ◽  
Vol 37 (8) ◽  
pp. 713-715 ◽  
Author(s):  
Shogo Tanaka ◽  
Daisuke Kubota ◽  
Sang Hum Lee ◽  
Kazuki Oba ◽  
Takatsugu Yamamoto ◽  
...  

2018 ◽  
Vol 34 (8) ◽  
pp. 1489-1495 ◽  
Author(s):  
Rohit Vadgaonkar ◽  
Sridhar Epari ◽  
Girish Chinnaswamy ◽  
Rahul Krishnatry ◽  
Raees Tonse ◽  
...  

2020 ◽  
Vol 11 (3) ◽  
pp. 364-365 ◽  
Author(s):  
Christopher R. Broda ◽  
Daniel A. Castellanos ◽  
Tam Dan N. Pham ◽  
W. Jeff Dreyer ◽  
Angeline D. Opina ◽  
...  

Fontan-associated protein-losing enteropathy is difficult to treat and associated with poor prognosis. Cardiac rehabilitation and exercise are thought to have beneficial effects for patients with Fontan circulation. We report the case of a young adult patient palliated to Fontan circulation, with a decade-long history of symptoms related to protein-losing enteropathy. At age 23 years, he appreciated an improvement in symptoms and laboratory values after cardiac rehabilitation and prescriptive exercise.


Sign in / Sign up

Export Citation Format

Share Document