scholarly journals Phylloid Hypermelanosis: An Unusual Form of Pigmentary Mosaicism

Dermatology ◽  
2010 ◽  
Vol 220 (2) ◽  
pp. 183-185 ◽  
Author(s):  
Rudolf Happle
Keyword(s):  
Unusual Form ◽  
Pigmentary Mosaicism

scholarly journals Necrotic plaques in an elderly male

JRSM Open ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 205427042098145
Author(s):  
Bindi Gaglani ◽  
Ian Logan ◽  
Faris Kubba
Keyword(s):  
Diabetes Mellitus ◽  
Genetic Predisposition ◽  
Unusual Case ◽  
Renal Diseases ◽  
Elderly Male ◽  
Unusual Form ◽  
Underlying Diseases ◽  
Reactive Perforating Collagenosis ◽  
Giant Form

Reactive perforating collagenosis is commonly recognised as an unusual form of transepithelial elimination of collagen and elastin fibres which are extruded through the epidermis in patients with a genetic predisposition or underlying diseases, such as diabetes mellitus or renal diseases. We present the unusual case of an 87-year-old diabetic male with a giant form of reactive perforating collagenosis and review the available literature.

Hemophagocytic Syndrome as an Unusual Form of Presentation of Tuberculosis in a Hemodialysis Patient

2000 ◽  
Vol 20 (3) ◽  
pp. 214-216 ◽  
Author(s):  
I. Castellano ◽  
J.R. Gómez-Martino ◽  
T. Hernández ◽  
L. Mateos ◽  
C. Argüello
Keyword(s):  
Hemophagocytic Syndrome ◽  
Hemodialysis Patient ◽  
Unusual Form

Unusual form of coarctation of the distal thoracic aorta

2001 ◽  
Vol 72 (4) ◽  
pp. 1395-1396 ◽  
Author(s):  
Rodolfo A Neirotti ◽  
Donald D Malcolm ◽  
George T Sugiyama ◽  
Gwendolyn R Fosse
Keyword(s):  
Thoracic Aorta ◽  
Unusual Form

104. On an Unusual Form of Tomahawk from Lake Superior.

Man ◽  
1907 ◽  
Vol 7 ◽  
pp. 182
Author(s):  
W. Crewdson
Keyword(s):  
Lake Superior ◽  
Unusual Form

An unusual form of Gaucher’s disease: pulmonary and cardiovascular involvement and cholelitiasis

Open Medicine ◽  
2010 ◽  
Vol 5 (4) ◽  
pp. 495-498
Author(s):  
Meltem Ceyhan ◽  
Fatma Celik ◽  
Muzaffer Elmali ◽  
Nevzat Gurmen
Keyword(s):  
High Resolution ◽  
Female Patient ◽  
Computerized Tomography ◽  
Storage Disease ◽  
Conventional Radiography ◽  
Gaucher's Disease ◽  
Gaucher’S Disease ◽  
High Resolution Ct ◽  
Unusual Form ◽  
Cardiovascular Involvement

AbstractGaucher’s disease is an inherited storage disease caused by a deficiency of the enzyme glucocerebrosidase. Although the hepatic manifestations are seen frequently, pulmonary and cardiovascular involvements are known to be very rare in Gaucher’s disease. This report presents these rare findings made by conventional radiography, computerized tomography (CT), and High-resolution CT (HRCT) of a 16-year-old female patient with fatal Gaucher’s disease.

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