Complete pachydermoperiostosis: A case report

被引:0
|
作者
Mubing, Mohd Firdaus Abdul [1 ]
Rahman, Razlina Abdul [1 ,2 ]
Badrin, Salziyan [1 ,2 ]
Ibrahim, Hasni [3 ]
机构
[1] Univ Sains Malaysia, Sch Med Sci, Dept Family Med, Kubang Kerian, Kelantan, Malaysia
[2] Hosp Univ Sains Malaysia, Jalan Raja Perempuan Zainab 2, Kubang Kerian, Kelantan, Malaysia
[3] Klin Kesihatan Gunong, Bachok, Kelantan, Malaysia
来源
关键词
cutis verticis gyrata; osteoarthropathy; pachydermoperiostosis; Touraine-Solente-Gole syndrome; PROSTAGLANDIN TRANSPORTER GENE; MUTATIONS; SLCO2A1; IDENTIFICATION;
D O I
10.29333/ejgm/13900
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pachydermoperiostosis (PDP), also known as Touraine-Solente-Gole syndrome or primary hypertrophic osteoarthropathy, is a very rare disease mainly characterized by pachyderma, finger clubbing, hyperhidrosis, and periostosis. We reported a case of a patient who suffered from gradual pain and enlargement of both hands and feet for 25 years despite receiving treatment from multiple clinics. He also experienced gradual abnormal changes in his face and scalp. Radiographic images of the lower limbs revealed the presence of subperiosteal bone growth and periosteal hypertrophy. The diagnosis of complete PDP was made late due to its rarity and the unfamiliarity of medical practitioners with the diagnosis. This case highlighted the need for medical practitioners to be aware of rare diseases so that patients may be diagnosed and treated earlier and thereby relieving their anxiety and improve their quality of life.
引用
收藏
页数:4
相关论文
共 50 条
  • [1] Primary Complete Pachydermoperiostosis: A Case Report
    Aliagaoglu, Cihangir
    Aslankurt, Murat
    Atasoy, Mustafa
    Onbas, Omer
    Bozkurt, Mahmut
    TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY, 2006, 40 : B20 - B22
  • [2] Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report
    Baniya, Abinash
    Bhattarai, Ayam
    Devkota, Bibek
    Khatiwada, Saurav
    Kafle, Pramod Kumar
    Phuyal, Achyut Krishna
    Shahi, Manoj
    CLINICAL CASE REPORTS, 2023, 11 (06):
  • [3] Complete primary pachydermoperiostosis: A case report from Jordan and review of literature
    Salah, Bareqa I.
    Husari, Khalil I.
    Hassouneh, Ala'
    Al-Ali, Zaid
    Rawashdeh, Baeth
    CLINICAL CASE REPORTS, 2019, 7 (02): : 346 - 352
  • [4] Complete form of pachydermoperiostosis in a 16-year-old boy: A case report
    Srinivas, Sahana
    Swamynathan, Suman
    Nagarajappa, Vani
    Palany, Raghupathy
    INDIAN JOURNAL OF PAEDIATRIC DERMATOLOGY, 2022, 23 (01) : 61 - 63
  • [5] PACHYDERMOPERIOSTOSIS (CASE-REPORT)
    CANCE, P
    BOUVIER, M
    LEJEUNE, E
    QUENEAU, P
    DAUMONT, A
    LLORCA, G
    LYON MEDICAL, 1977, 238 (17): : 293 - 297
  • [6] Pachydermoperiostosis. A case report
    Kabi, F.
    Mkinsi, O.
    Janani, S.
    Raissouni, N.
    REVUE DE MEDECINE INTERNE, 2006, 27 (09): : 710 - 712
  • [7] A complicated case of pachydermoperiostosis with spondyloarthritides: A case report
    Zhang Q.
    Shen M.
    Yang B.
    Yu K.
    Journal of Medical Case Reports, 7 (1)
  • [8] Pachydermoperiostosis Mimicking Acromegaly: A Case Report
    Kwon, Mi-Hye
    Joung, Chung-Il
    TURKISH JOURNAL OF RHEUMATOLOGY, 2012, 27 (02) : 132 - 135
  • [9] Pachydermoperiostosis and Work Restrictions: A Case Report
    Chinichian, Mahdi
    Asghari, Omid
    Safaie, Niloofar
    Kassiri, Negin
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2023, 15 (03)
  • [10] Complete form of pachydermoperiostosis
    Padilha Honorio, Monica Larissa
    Bezerra, Guilherme Holanda
    da Camara Costa, Vivianne Lira
    ANAIS BRASILEIROS DE DERMATOLOGIA, 2020, 95 (01) : 98 - 101