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Indurated Plaque With Ulceration on the Dorsum of the Left Hand

Educational Objective
Based on this clinical scenario and the accompanying image, understand how to arrive at a correct diagnosis.
1 Credit CME

A man in his 70s presented with a 6-month history of a rash on the left forearm, which gradually increased in severity. The patient developed a rash on the dorsal aspect of his hand half a year ago without any pain or itching discomfort and denied any history of injury or exposure to suspected pathogens prior to onset. After self-medication with topical herbal medicine, the lesions gradually spread to the forearm and fused into plaques, and ulcers often recurred on the surface. He denied any systemic symptoms and concerns. Physical examination revealed large, firm, mildly swollen erythematous plaques on the back of the left forearm with purulent discharge and crusting (Figure, A). Results of routine laboratory investigations, including complete blood cell count, biochemical profile, and chest radiography, were normal. A biopsy specimen was taken for pathological examination (Figure, B-D).

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C. Cutaneous protothecosis

Hyperkeratosis, pseudoepitheliomatous hyperplasia, and a lymphohistiocytic infiltrate with granuloma formation, neutrophils, plasma cells, and multinucleated giant cells in the dermis were observed in the pathological examination (Figure, B). Periodic acid–Schiff staining showed mulberrylike thick-walled spherical or ovoid spores of various sizes and high-density cell walls (Figure, C). Multiple endospores were highlighted by transmission electron microscopy and were irregular asexually separated schizonts (Figure, D). After identification of Protothecosis wickerhamii by molecular sequencing technology, the diagnosis of protothecosis was confirmed. One month after oral administration of itraconazole, 0.2 g, every day, the patient’s rash subsided considerably.

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Article Information

Corresponding Author: Borui Chen, MD, PhD, Dermatology Institute of Fuzhou, Dermatology Hospital of Fuzhou, Xihong Rd 243, Fuzhou 350025, China (pekking@gmail.com).

Published Online: November 9, 2022. doi:10.1001/jamadermatol.2022.4889

Conflict of Interest Disclosures: None reported.

Additional Contributions: We thank the patient for granting permission to publish this information. We also thank Jun Chen, MD, Liqiang Weng, MD, and Qinqin Long, MD, all from the Dermatology Hospital of Fuzhou, for their assistance in pathology; Wanding Lu, MD, from the Dermatology Hospital of Fuzhou, for assisting in professional guidance and comments on this case; and Xi Lin, MS, from the Public Technology Service Center of Fujian Medical University, for support in transmission electron microscopy. They were not compensated for their contributions.

References
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Davies  RR , Spencer  H , Wakelin  PO .  A case of human protothecosis.   Trans R Soc Trop Med Hyg. 1964;58(5):448-451. doi:10.1016/0035-9203(64)90094-XPubMedGoogle ScholarCrossref
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Okuyama  Y , Hamaguchi  T , Teramoto  T , Takiuchi  I .  A human case of protothecosis successfully treated with itraconazole.   Nihon Ishinkin Gakkai Zasshi. 2001;42(3):143-147. doi:10.3314/jjmm.42.143PubMedGoogle ScholarCrossref
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Seok  JY , Lee  Y , Lee  H , Yi  SY , Oh  HE , Song  JS .  Human cutaneous protothecosis: report of a case and literature review.   Korean J Pathol. 2013;47(6):575-578. doi:10.4132/KoreanJPathol.2013.47.6.575PubMedGoogle ScholarCrossref
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Queiroz-Telles  F , de Hoog  S , Santos  DW ,  et al.  Chromoblastomycosis.   Clin Microbiol Rev. 2017;30(1):233-276. doi:10.1128/CMR.00032-16PubMedGoogle ScholarCrossref
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McGinnis  MR .  Chromoblastomycosis and phaeohyphomycosis: new concepts, diagnosis, and mycology.   J Am Acad Dermatol. 1983;8(1):1-16. doi:10.1016/S0190-9622(83)70001-0PubMedGoogle ScholarCrossref
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Noguchi  H , Matsumoto  T , Kimura  U , Hiruma  M , Kusuhara  M , Ihn  H .  Cutaneous cryptococcosis.   Med Mycol J. 2019;60(4):101-107. doi:10.3314/mmj.19.008PubMedGoogle ScholarCrossref
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Sainz-Gaspar  L , Rosón  E , Llovo  J , Vázquez-Veiga  H .  Photodynamic therapy in the treatment of cutaneous leishmaniasis.   Actas Dermosifiliogr (Engl Ed). 2019;110(3):249-251. doi:10.1016/j.ad.2018.02.018PubMedGoogle ScholarCrossref
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Von Stebut  E .  Leishmaniasis.   J Dtsch Dermatol Ges. 2015;13(3):191-200. doi:10.1111/ddg.12595PubMedGoogle ScholarCrossref
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Bakuła  Z , Siedlecki  P , Gromadka  R ,  et al.  A first insight into the genome of Prototheca wickerhamii, a major causative agent of human protothecosis.   BMC Genomics. 2021;22(1):168. doi:10.1186/s12864-021-07491-8PubMedGoogle ScholarCrossref
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AMA CME Accreditation Information

Credit Designation Statement: The American Medical Association designates this Journal-based CME activity activity for a maximum of 1.00  AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to:

  • 1.00 Medical Knowledge MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program;;
  • 1.00 Self-Assessment points in the American Board of Otolaryngology – Head and Neck Surgery’s (ABOHNS) Continuing Certification program;
  • 1.00 MOC points in the American Board of Pediatrics’ (ABP) Maintenance of Certification (MOC) program;
  • 1.00 Lifelong Learning points in the American Board of Pathology’s (ABPath) Continuing Certification program; and
  • 1.00 CME points in the American Board of Surgery’s (ABS) Continuing Certification program

It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting MOC credit.

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