scholarly journals Respiratory manifestation of yellow nail syndrome: a case report and literature review

2021 ◽  
Vol 49 (12) ◽  
pp. 030006052110633
Author(s):  
Shan Xu ◽  
Xiaohong Wu

Yellow nail syndrome (YNS) is a rare disorder, and diagnosis is based on the clinical findings and the exclusion of other possible causes; the pathogenesis is poorly understood. YNS can be an isolated condition or associated with other diseases; however, YNS associated with multiple myeloma (MM) is rare. A 53-year-old male patient presented with coughing and shortness of breath, and he was diagnosed with YNS with MM. He underwent chemotherapy and achieved a good response. Although the etiology of YNS remains unknown, treating the underlying disease may help prevent or relieve the clinical signs.

2019 ◽  
Vol 11 (3) ◽  
pp. 278-285
Author(s):  
Kanchana Leerunyakul ◽  
Phatcharawat Chirasuthat ◽  
Poonkiat Suchonwanit

Follicular hyperkeratotic spicules is a rare skin disorder that is usually associated with multiple myeloma. The condition typically presents with tiny hyperkeratotic spicules in follicular distribution and predominantly on the face. To our knowledge, there has been one reported case of this condition without underlying disease. We herein report the second case of idiopathic follicular hyperkeratotic spicules in a 54-year-old Thai woman presenting with multiple follicular horn-like spicules on her face and neck.


1993 ◽  
Vol 34 (3) ◽  
pp. 293 ◽  
Author(s):  
Philip J. Klenn ◽  
Bong H. Hyun ◽  
Young Hee Lee ◽  
Wen Yu Zheng

2006 ◽  
Vol 16 (S3) ◽  
pp. 242-249 ◽  
Author(s):  
Miriam Rodriguez-Catarino ◽  
Cecilie Blimark ◽  
Jan Willén ◽  
Ulf-H Mellqvist ◽  
Stig Rödjer

2005 ◽  
Vol 84 (6) ◽  
pp. 358-361 ◽  
Author(s):  
Sandra Doria Xavier ◽  
Ivo Bussoloti Filho ◽  
Helena Müller

Amyloidosis is characterized by an abnormal extracellular deposition of amyloid in different tissues and organs, where it usually causes some type of dysfunction. Its cause is unknown. The two main forms of amyloidosis are systemic and localized; the latter is rare. No satisfactory treatment for systemic amyloidosis has been discovered, and mean survival is poor, ranging from 5 to 15 months depending on the presence or absence of multiple myeloma. We report a case of primary systemic amyloidosis in a 71-year-old man. The diagnosis of amyloidosis was established by tongue biopsy, and its systemic nature was identified by analysis of aspirated abdominal fat. At the 1-year follow-up, the patient's clinical condition had not changed, and he was thereafter lost to follow-up.


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