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Journal articles on the topic 'Keratoderma palmoplantar'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 February 2022

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1

Dessureault, Josee, Yves Poulin, Marc Bourcier, and Eric Gagne. "Olmsted Syndrome—Palmoplantar and Periorificial Keratodermas: Association with Malignant Melanoma." Journal of Cutaneous Medicine and Surgery 7, no. 3 (2003): 236–42. http://dx.doi.org/10.1177/120347540300700309.

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Background: Olmsted syndrome is a rare congenital disorder with mutilating palmoplantar keratoderma, periorificial keratotic plaques, and other variable features. Objective: We describe a 65-year-old woman with Olmsted syndrome complicated by the occurrence of a malignant melanoma inside the plantar keratoderma. To our knowledge, this is the first reported case of such an occurrence in Olmsted syndrome. The published cases of this rare disorder are reviewed. Conclusion: An association between malignant epithelial tumors and Olmsted syndrome has already been reported. The association of malignant melanoma with other types of palmoplantar keratodermas has been reported. This may suggest a predisposition to melanocytic as well as squamous cell malignancies in congenital keratodermas. Oral retinoids appear to be the most promising treatment for Olmsted syndrome and for other symptomatic keratodermas.

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2

Bhansali, Ashok, Setu Mathur, Gunjan Bhansali, and Anuroopa Kishan. "Palmoplantar Keratoderma with Periodontitis." Journal of Health Sciences & Research 8, no. 2 (2017): 89–92. http://dx.doi.org/10.5005/jp-journals-10042-1057.

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ABSTRACT Palmoplantar keratodermas (PPKs) comprise a heterogeneous group of keratinization disorders with hyperkeratotic thickening of palms and soles. The PPKs are distinguished by their mode of inheritance and by the presence of certain associated clinical features. Periodontitis was reported in association with more than one syndrome characterized by PPK. Knowledge about heterogeneous groups of acquired or hereditary PPK is important, leading to an appropriate diagnosis and corrective therapies in the future. This case report aims at critically reviewing the literature concerned with PPK and its clinical presentation, in addition to other syndromes manifested along with periodontitis. How to cite this article Bhansali A, Kishan A, Mathur S, Bhansali G. Palmoplantar Keratoderma with Periodontitis. J Health Sci Res 2017;8(2):89-92.

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3

OʼConnor, Elizabeth A., and William W. Dzwierzynski. "Palmoplantar Keratoderma." Annals of Plastic Surgery 67, no. 4 (2011): 439–41. http://dx.doi.org/10.1097/sap.0b013e3182085a8b.

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4

Lestre, Sara, Eva Lozano, Cláudia Meireles, and Ana Barata Feio. "Autoimmune Thyroiditis Presenting as Palmoplantar Keratoderma." Case Reports in Medicine 2010 (2010): 1–3. http://dx.doi.org/10.1155/2010/604890.

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Palmoplantar keratoderma is a heterogeneous group of hereditary and acquired disorders characterized by abnormal thickening of palms and soles. Hypothyroidism is an unusual cause of palmoplantar keratoderma, rarely reported in the literature. We report a case of a 43-year-old woman presented with a 3-month history of a diffuse palmoplantar hyperkeratosis unresponsive to topical keratolytics and corticosteroids. Her past medical and family histories were unremarkable. She complained of recent asthenia, mood changes and constipation. Laboratory evaluation revealed an autoimmune thyroiditis with hypothyroidism. Other causes of acquired palmoplantar keratoderma were excluded. After hormonal replacement therapy institution, a gradual improvement of skin condition was observed. The diagnosis of underlying causes for acquired palmoplantar keratoderma can be a difficult task; however its recognition is essential for successful treatment results. Although a very rare association, hypothyroidism must be suspected in patients with acquired palmoplantar keratoderma, particularly when it occurs in association with systemic symptoms.

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5

USUKI, Kazunari. "Aquagenic Palmoplantar Keratoderma." Nishi Nihon Hifuka 65, no. 5 (2003): 443–45. http://dx.doi.org/10.2336/nishinihonhifu.65.443.

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6

KAWAI, Kazuhiro, Tomoko FUKUSHIGE, Masanao SAKANOUE, and Takuro KANEKURA. "Striate palmoplantar keratoderma." Journal of Dermatology 37, no. 9 (2010): 854–56. http://dx.doi.org/10.1111/j.1346-8138.2010.00874.x.

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7

Yan, Albert C., Sumaira Z. Aasi, William J. Alms, et al. "Aquagenic palmoplantar keratoderma." Journal of the American Academy of Dermatology 44, no. 4 (2001): 696–99. http://dx.doi.org/10.1067/mjd.2001.113479.

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8

Patel, Shaily, Matthew Zirwas, and Joseph C. English. "Acquired Palmoplantar Keratoderma." American Journal of Clinical Dermatology 8, no. 1 (2007): 1–11. http://dx.doi.org/10.2165/00128071-200708010-00001.

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9

Imbernón-Moya, A., A. Aguilar-Martínez, and E. Vargas-Laguna. "Linear Palmoplantar Keratoderma." Actas Dermo-Sifiliográficas (English Edition) 109, no. 3 (2018): 269. http://dx.doi.org/10.1016/j.adengl.2018.02.014.

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10

Bukhari, Rahaf, Waseem Alhawsawi, Aisha Ahmad Radin, Hawazin D. Jan, Khalid Al Hawsawi, and Marwan Al Ahmadi. "Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease)." Case Reports in Dermatology 11, no. 3 (2019): 292–96. http://dx.doi.org/10.1159/000503337.

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Punctate palmoplantar keratoderma is a rare hereditary palmoplantar keratoderma. Herein we report a 59-year-old male, otherwise healthy, who presented with a 25-year history of asymptomatic persistent slowly progressing skin lesions on both hands. The parents are non-consanguineous and none of his family members had similar lesions. Skin examination revealed multiple tiny keratotic pits on both palms. Punch skin biopsy from the palmar lesion revealed epidermal depression with an overlying column of compact orthokeratosis. Based on the above clinicopathological findings, a diagnosis of punctate palmoplantar keratoderma type 1 was made. The patient was started on 40% urea and 20% salicylic acid ointment for months but with little improvement.

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11

Gupta, VedPrakash, and Isha Chaudhari. "Palmoplantar keratoderma with keratoconus." Middle East African Journal of Ophthalmology 25, no. 1 (2018): 49. http://dx.doi.org/10.4103/meajo.meajo_221_17.

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12

Chen, K. L., Y. T. Cho, C. W. Yang, et al. "Olmutinib-induced palmoplantar keratoderma." British Journal of Dermatology 178, no. 2 (2017): e129-e131. http://dx.doi.org/10.1111/bjd.15935.

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13

Lee Dellon, A. "Epidermalytic hereditary palmoplantar keratoderma." Journal of Hand Surgery 16, no. 1 (1991): 180. http://dx.doi.org/10.1016/s0363-5023(10)80040-1.

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14

Fonseca, E. "Epidermolytic hereditary palmoplantar keratoderma." British Journal of Dermatology 113, no. 4 (1985): 505. http://dx.doi.org/10.1111/j.1365-2133.1985.tb02371.x.

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15

Jacyk, W. K., and P. L. Bill. "Palmoplantar Keratoderma with Amyotrophy." Dermatology 176, no. 5 (1988): 251–56. http://dx.doi.org/10.1159/000248713.

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16

Xoagus, Elizabeth, Donald Hudson, and Sean Moodley. "Palmoplantar keratoderma surgical management." Journal of Plastic, Reconstructive & Aesthetic Surgery 67, no. 12 (2014): e316-e317. http://dx.doi.org/10.1016/j.bjps.2014.08.012.

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17

Swetha, Sridhar, Samayam Aneesh, and Anjan Kumar Patra. "A rare case of Vohwinkel’s syndrome." Our Dermatology Online 11, e (2020): e183.1-e183.3. http://dx.doi.org/10.7241/ourd.2020e.183.

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Keratoderma hereditarium mutilans or Vohwinkel’s syndrome is a rare autosomal dominant type of palmoplantar keratoderma characterized by honeycomb appearance, pseudoainhum leading to auto-amputation and stellate keratosis on knuckles. It’s mode of inheritance is autosomal dominant with mutation in loricrin and connexin 26 genes. We report the case of a 35-year-old female with alopecia universalis since birth and transgradient palmoplantar keratoderma, impaired hearing and pseudoainhum formation since childhood. This case is being reported to highlight the association of Vohwinkel’s syndrome with sensorineural hearing loss and alopecia universalis.

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18

MORI, Makiko, Noriyuki HIRASHIMA, Masakazu OHTSU, et al. "Aquagenic Palmoplantar Keratoderma : A Report of Five Cases." Nishi Nihon Hifuka 76, no. 6 (2014): 555–61. http://dx.doi.org/10.2336/nishinihonhifu.76.555.

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19

Tiwary, AnupKumar, Sagarika Chatterjee, and DharmendraKumar Mishra. "Brunauer–Fuhs–Siemens palmoplantar keratoderma: A rare, striate type of focal palmoplantar keratoderma." Indian Journal of Paediatric Dermatology 17, no. 3 (2016): 246. http://dx.doi.org/10.4103/2319-7250.179500.

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20

Hashimoto, T., K. Teye, S. Numata, Y. Suga, T. Hamada, and N. Ishii. "Detection ofSERPINB7mutation can distinguish Nagashima-type palmoplantar keratoderma from other keratodermas with palmoplantar lesions." Clinical and Experimental Dermatology 42, no. 3 (2017): 342–45. http://dx.doi.org/10.1111/ced.13059.

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21

Almutawa, Fahad, Thusanth Thusaringam, Kevin Watters, Tenzin Gayden, Nada Jabado, and Denis Sasseville. "Pachyonychia Congenita (K16) with Unusual Features and Good Response to Acitretin." Case Reports in Dermatology 7, no. 2 (2015): 220–26. http://dx.doi.org/10.1159/000438920.

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Background: Pachyonychia congenita (PC) is a rare autosomal dominant disease whose main clinical features include hypertrophic onychodystrophy and palmoplantar keratoderma. The new classification is based on genetic variants with mutations in keratin KRT6A, KRT6B, KRT6C, KRT16, KRT17, and an unknown mutation. Here, we present a case of PC with unusual clinical and histological features and a favorable response to oral acitretin. Case: A 49-year-old male presented with diffuse and striate palmoplantar keratoderma, thickened nails, knuckle pads, and pseudoainhum. Histology showed compact hyperkeratosis, prominent irregular acanthosis, and extensive epidermolytic hyperkeratosis, suggestive of Vörner's palmoplantar keratoderma. However, keratin 9 and 1 were not mutated, and full exome sequencing showed heterozygous missense mutation in type I keratin K16. Conclusion: To our knowledge, epidermolytic hyperkeratosis has not been previously described with PC. Our patient had an excellent response, maintained over the last 5 years, to a low dose of acitretin. We wish to emphasize the crucial role of whole exome sequencing in establishing the correct diagnosis.

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22

Singh, MP, Manishi Singh, Manika Singh, and Prashant Tripathi. "Clouston Syndrome with Palmoplantar Keratoderma." Journal of Indian Academy of Oral Medicine and Radiology 23 (July 2011): S425—S428. http://dx.doi.org/10.5005/jp-journals-10011-1188.

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23

Kaliyadan, Feroze, and Ajit Nambiar. "Palmoplantar keratoderma with dental abnormalities." Indian Dermatology Online Journal 5, no. 2 (2014): 232. http://dx.doi.org/10.4103/2229-5178.131152.

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24

Itin, Peter H., and Stephan Lautenschlager. "Palmoplantar keratoderma and associated syndromes." Seminars in Dermatology 14, no. 2 (1995): 152–61. http://dx.doi.org/10.1016/s1085-5629(05)80012-4.

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25

Yilmaz, P., M. Medvecz, J. Kohlhase, J. Küsel, J. Fischer, and C. Has. "Alitretinoin in punctate palmoplantar keratoderma." British Journal of Dermatology 180, no. 4 (2018): 931–32. http://dx.doi.org/10.1111/bjd.17336.

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26

Sehgal, Virendra N., Devinder M. Thappa, and Sanjiv Jain. "Palmoplantar Keratoderma with Cutaneous Horns." International Journal of Dermatology 31, no. 5 (1992): 369–70. http://dx.doi.org/10.1111/j.1365-4362.1992.tb03967.x.

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27

Nielsen, Povl Gamborg. "Hereditary Palmoplantar Keratoderma and Dermatophytosis." International Journal of Dermatology 27, no. 4 (1988): 223–31. http://dx.doi.org/10.1111/j.1365-4362.1988.tb03213.x.

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28

Alsaleh, Q. A., and A. S. Teebi. "Autosomal recessive epidermolytic palmoplantar keratoderma." Journal of Medical Genetics 27, no. 8 (1990): 519–22. http://dx.doi.org/10.1136/jmg.27.8.519.

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29

FITZGERALD, D. A., and J. L. VERBOV. "Hereditary palmoplantar keratoderma with deafness." British Journal of Dermatology 134, no. 5 (1996): 939–42. http://dx.doi.org/10.1111/j.1365-2133.1996.tb06331.x.

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30

FITZGERALD, D. A., and J. L. VERBOV. "Hereditary palmoplantar keratoderma with deafness." British Journal of Dermatology 134, no. 5 (1996): 939–42. http://dx.doi.org/10.1046/j.1365-2133.1996.133868.x.

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31

Miller, Roling, Spiers, Davies, Rawlings, and Leyden. "Palmoplantar keratoderma associated with hypothyroidism." British Journal of Dermatology 139, no. 4 (1998): 741–42. http://dx.doi.org/10.1046/j.1365-2133.1998.02480.x.

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32

Singh, Sanjay, Prateek Sondhi, and Gomathy Sethuraman. "Palmoplantar keratoderma with curly hair." Pediatric Dermatology 34, no. 6 (2017): 724–25. http://dx.doi.org/10.1111/pde.13307.

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33

Verbov, J. "Palmoplantar keratoderma, deafness and atopy." British Journal of Dermatology 116, no. 6 (1987): 881. http://dx.doi.org/10.1111/j.1365-2133.1987.tb04914.x.

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34

Wevers, Andrea, Andreas Kuhn, and Gustav Mahrle. "Palmoplantar keratoderma with tonotubular keratin." Journal of the American Academy of Dermatology 24, no. 4 (1991): 638–42. http://dx.doi.org/10.1016/0190-9622(91)70099-n.

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35

Das, Anupam, Dhiraj Kumar, and Nilay Kanti Das. "Diffuse non-epidermolytic Palmoplantar Keratoderma." Indian Pediatrics 50, no. 10 (2013): 979. http://dx.doi.org/10.1007/s13312-013-0249-z.

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36

Barman, KrishnaDeb, Sudhanshu Sharma, VijayKumar Garg, and Shalu Jain. "Unilateral linear punctate palmoplantar keratoderma." Indian Journal of Dermatology, Venereology, and Leprology 78, no. 1 (2012): 85. http://dx.doi.org/10.4103/0378-6323.90953.

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37

Jha, Niharika, Bimal Kanish, and Anuradha Bhatia. "Imatinib mesylate-induced palmoplantar keratoderma." Indian Journal of Drugs in Dermatology 7, no. 1 (2021): 49. http://dx.doi.org/10.4103/ijdd.ijdd_17_20.

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38

Foy, Hjordis M., Samran Tarmapai, Poovanon Eamchan, and Orapun Metdilogkul. "Chronic Arsenic Poisoning from Well Water in a Mining Area in Thailand." Asia Pacific Journal of Public Health 6, no. 3 (1992): 150–52. http://dx.doi.org/10.1177/101053959200600306.

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Endemic arsenic poisoning manifested by palmoplantar keratoderma and hyperpigmentation was surveyed in a village in a tin and wolfram mining area in southern Thailand where two cases of Bowen's carcinoma had occurred. Nine percent of examined adults randomly selected from 58 households were found to have skin manifestations of arsenic poisoning. Also, children with typical palmoplantar keratoderma were recognized, the youngest being four years old. A seven-year-old with severe keratoderma also had neurological manifestations and appeared mentally retarded. Arsenic concentration in shallow wells varied between 0.02-2.7 mg/1 (average 0.82), and piped water had 0.07 mg/1. A major source of the contamination of ground water probably was slag heaps positioned next to a stream that led the village.

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39

M., Geetha, Rajeswari Bhat, Kiran B., Madhusmitha Jena, and Libni D. Angel. "Unna Thost syndrome: a case report." International Journal of Contemporary Pediatrics 6, no. 4 (2019): 1767. http://dx.doi.org/10.18203/2349-3291.ijcp20192793.

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Unna thost syndrome is Palmo Plantar Keratoderma (PPK) of diffuse non epidermolytic type inherited in autosomal dominant fashion. Authors had a seven-year-old boy born to second degree consanguineous parents had palmoplantar keratoderma with hyperhidrosis with positive family history. He was promptly diagnosed and treated with acitretin and showed improvement.

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40

Hamm, H., R. Happle, T. Butterfass, and H. Traupe. "Epidermolytic Palmoplantar Keratoderma of Vörner: Is It the Most Frequent Type of Hereditary Palmoplantar Keratoderma?" Dermatology 177, no. 3 (1988): 138–45. http://dx.doi.org/10.1159/000248531.

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41

Pashinyan, Albina G., L. I. Ilienko, and A. N. Akopyan. "CLINICAL CASE OF PALMOPLANTAR KERATODERMA TYPE UNNA-THOST." Russian Journal of Skin and Venereal Diseases 20, no. 3 (2017): 143–45. http://dx.doi.org/10.18821/1560-9588-2017-20-3-143-145.

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Palmar-plantar keratoderma is a heterogeneous group of hereditary dermatosis, which can be independent diseases or combined with various congenital malformations, most of ectodermal origin. Approaches to differential diagnosis and clinical features of each form of this pathology are described. Keratoderma, Unna Toast genodermatosis belongs to the group, which is characterized by hyperkeratosis on the palms and soles without migration to other skin areas.

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42

Kaliuzhna, L. D., та A. V. Petrenko. "Редкий вариант ладонно-подошвенной кератодермии". Dermatology and Venerology, № 3 (9 жовтня 2019): 39–40. http://dx.doi.org/10.33743/2308-1066-2019-3-39-40.

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43

Mathon, Shivanu, and Manu Singh. "A Review on Hereditary Palmoplantar Keratoderma." Scholars Journal of Applied Medical Sciences 08, no. 03 (2020): 821–26. http://dx.doi.org/10.36347/sjams.2020.v08i03.011.

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44

FUKUSHIMA, Satoshi, Mika KINOSHITA, Junko HIGO, Masato KIDOU, Fukiko AMANO, and Tomomichi ONO. "A Case of Aquagenic Palmoplantar Keratoderma." Nishi Nihon Hifuka 64, no. 6 (2002): 693–97. http://dx.doi.org/10.2336/nishinihonhifu.64.693.

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45

TÜRKMEN, Dursun, Kısmet KAYA, and Özlem SEZER. "Two Cases with Aquagenic Palmoplantar Keratoderma." Turkiye Klinikleri Journal of Case Reports 26, no. 3 (2018): 130–33. http://dx.doi.org/10.5336/caserep.2017-58582.

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46

Kanitakis, Jean, George Tsoitis, and Constantine Kanitakis. "Hereditary epidermolytic palmoplantar keratoderma (Vörner type)." Journal of the American Academy of Dermatology 17, no. 3 (1987): 414–22. http://dx.doi.org/10.1016/s0190-9622(87)70222-9.

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47

Rapprich, Stefan, and Manfred Hagedorn. "Surgical treatment of severe palmoplantar keratoderma." JDDG: Journal der Deutschen Dermatologischen Gesellschaft 9, no. 3 (2010): 252–55. http://dx.doi.org/10.1111/j.1610-0387.2010.07579.x.

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48

Yoshikawa, Yoshiaki, Toshihiro Tanaka, Ken-ichi Toda, and Yoshiki Miyachi. "A Unique Case of Palmoplantar Keratoderma." Journal of Dermatology 30, no. 10 (2003): 755–57. http://dx.doi.org/10.1111/j.1346-8138.2003.tb00473.x.

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49

Khamaysi, Z., M. Indelman, R. Bergman, and E. Sprecher. "Familial palmoplantar keratoderma: not always hereditary." Journal of the European Academy of Dermatology and Venereology 21, no. 10 (2007): 1437–38. http://dx.doi.org/10.1111/j.1468-3083.2007.02251.x.

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50

Oiso, N., S. Kawara, and A. Kawada. "Focal palmoplantar keratoderma with epidermolytic degeneration." Journal of the European Academy of Dermatology and Venereology 23, no. 5 (2009): 570–71. http://dx.doi.org/10.1111/j.1468-3083.2008.02857.x.

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