Congenital Cutis Verticis Gyrata in a Newborn with Turner Syndrome: A Rare Clinical Manifestation of This Chromosomal Disease with Trichoscopic Evaluation

被引:0
|
作者
Bortone, Riccardo [1 ]
Bonamonte, Domenico [1 ]
Cazzato, Gerardo [2 ]
Laface, Carmelo [3 ]
Gaeta, Alberto [4 ]
Lettini, Teresa [1 ]
Foti, Caterina [1 ]
Filotico, Raffaele [1 ]
Ambrogio, Francesca [1 ]
机构
[1] Univ Bari Aldo Moro, Dept Precis & Regenerat Med & Ionian Area DiMePRe, Sect Dermatol & Venereol, I-70124 Bari, Italy
[2] Univ Bari Aldo Moro, Dept Precis & Regenerat Med & Ionian Area DiMePRe, Sect Mol Pathol, I-70124 Bari, Italy
[3] Dario Camberlingo Hosp, Med Oncol, I-72021 Francavilla Fontana, Italy
[4] Pediat Hosp Giovanni XXIII, Radiol Unit, I-70126 Bari, Italy
关键词
congenital cutis verticis gyrate; Turner syndrome; chromosomal disease; trichoscopy;
D O I
10.3390/diagnostics13152574
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cutis verticis gyrata (CVG) is a rare disorder of the scalp that entails the development of ridges and furrows, which mimic the anatomical conformation of the brain. This skin condition has been classified in primary essential, primary non-essential, and secondary CVG, depending on the presence or absence of other associated disorders. We present the case report of a one-month-old female newborn affected by congenital CVG (CCVG), who also received a diagnosis of Turner syndrome (TS). Skin folding was present at birth and located at the left frontal region of the scalp in the sagittal plane. Our purpose was to make this pathology clinically and tricoscopically better known, since it can be related to different genetic, inflammatory, and neoplastic conditions, etc. Non-invasive investigations, such as ultrasonography (U/S) of the brain and scalp and trichoscopy, were also used to obtain the important clues necessary to help in the CVG classification. The clinical diagnosis and trichoscopical investigation of CVG may also be useful for those patients who may have a genetic disease that is not screened for during prenatal examinations.
引用
收藏
页数:6
相关论文
共 19 条
  • [1] Clinical insights from an unusual Turner syndrome manifestation: Congenital cutis verticis gyrata
    Roman Corona-Rivera, Jorge
    Bustos Rodriguez, Felipe de Jesus
    Leticia Vega-Silva, Laura
    Hernandez-Camarena, Fernando
    Pena-Padilla, Christian
    Alejandra Castillo-Reyes, Katia
    Paola Cruz-Cruz, Jessica
    Bobadilla-Morales, Lucina
    Corona-Rivera, Alfredo
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191 (06) : 1669 - 1671
  • [2] Cutis verticis gyrata in a child with Turner syndrome
    Marinoni, LP
    Taniguchi, K
    Giraldi, S
    Carvalho, VO
    Furucho, M
    Bertogna, J
    [J]. PEDIATRIC DERMATOLOGY, 1999, 16 (03) : 242 - 243
  • [3] Cutis Verticis Gyrata: A Rare Cutaneous Presenting Manifestation of Acromegaly
    Arjunan, Durairaj
    Das, Liza
    Bhadada, Sanjay K.
    Tripathi, Manjul
    Narang, Tarun
    Dutta, Pinaki
    [J]. INDIAN JOURNAL OF DERMATOLOGY, 2023, 68 (05)
  • [4] Lymphedema as a postulated cause of cutis verticis gyrata in Turner syndrome
    Larralde, M
    Gardner, SS
    Torrado, MD
    Fernhoff, PM
    Munoz, AES
    Spraker, MK
    Sybert, VP
    [J]. PEDIATRIC DERMATOLOGY, 1998, 15 (01) : 18 - 22
  • [5] Cutis verticis gyrata associated with congenital heart disease
    Teresa-Palacio, Marta
    Akpoke, Michael Agwu
    Bah, Abubakarr Bailor
    Aldecoa-Bilbao, Victoria
    [J]. BMJ CASE REPORTS, 2024, 17 (02)
  • [6] Diagnostic challenge of cutis Verticis Gyrata (CVG) in a patient presenting clinical features of Noonan or turner syndrome
    Kanotra, Muskan
    Kaur, Rupinder
    Pasricha, Chirag
    Kumari, Pratima
    Singh, Ravinder
    Singh, Varinder
    Ahmad, Sheikh F.
    [J]. MOLECULAR GENETICS AND METABOLISM REPORTS, 2024, 41
  • [7] Congenital leukemia cutis: An unusual manifestation of a rare disease
    Campbell, DC
    Grippaudo, FR
    Lewandowski, R
    [J]. PLASTIC AND RECONSTRUCTIVE SURGERY, 1997, 100 (07): : 1809 - 1811
  • [8] A RARE FORM OF CONGENITAL HEART-DISEASE AND TURNER SYNDROME
    BLUMENTHAL, D
    KURER, CC
    FOX, JE
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 257 - 257
  • [9] TURNER PHENOTYPE WITH NORMAL SEX CHROMOSOMAL PATTERN AND CONGENITAL HEART-DISEASE (NOONANS SYNDROME)
    VANDERHORST, RL
    [J]. SOUTH AFRICAN MEDICAL JOURNAL, 1974, 48 (06): : 219 - 222
  • [10] A RARE CLINICAL MANIFESTATION OF GRAVES' DISEASE: EVANS SYNDROME AND A REVIEW OF THE LITERATURE
    Calapkulu, M.
    Sencar, M. E.
    Yildiz, A.
    Unsal, I. O.
    Cakal, E.
    [J]. ACTA ENDOCRINOLOGICA-BUCHAREST, 2020, 16 (04) : 518 - 521