Acquired cutis laxa secondary to Sweet syndrome in a child (Marshall syndrome): A rare case report

2019 ◽  
Vol 47 (2) ◽  
pp. 146-149
Author(s):  
Ashish Jagati ◽  
Shivank Shrivastava ◽  
Bhavna Baghela ◽  
Pooja Agarwal ◽  
Siddhartha Saikia
2021 ◽  
Vol 7 (3) ◽  
pp. 268-271
Author(s):  
R Roja ◽  
Ramanamurthy Pemmaraju ◽  
Krishnarao V Pasagadugula ◽  
Raajitha N S S Penugonda

Elastosis perforans serpiginous (EPS) is a rare perforating disorder characterized by trans epidermal elimination of fragmented elastic fibres.The cutaneous features include asymptomatic hyperkeratotic papules. Here we present a case of 27-year old female presented with hyperkeratotic papules with central depression arranged transversely in a serpiginous fashion on front of the laxed skin of the neck region. The histopathological features are consistent with the features of EPS on Cutis Laxa. Elastosis perforans serpiginosa in Acquired cutis laxa has not been reported very rarely, hence this case has been reported.


2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko

Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  

2011 ◽  
Vol 3 (6) ◽  
pp. 405-406
Author(s):  
Dr. Nale Swati S Dr. Nale Swati S ◽  
◽  
Dr.Ghadage Dnyaneshwari P ◽  
Bhore Arvind V

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