Literature DB >> 28584771

SkIndia Quiz 38: Subcutaneous Thumb Tumor.

Sylvia Aide Martínez-Cabriales1, Osvaldo Tomás Vázquez-Martínez1, Guillermo Antonio Guerrero-González1, Jorge Ocampo-Candiani1.   

Abstract

Entities:  

Year:  2017        PMID: 28584771      PMCID: PMC5447354          DOI: 10.4103/2229-5178.202363

Source DB:  PubMed          Journal:  Indian Dermatol Online J        ISSN: 2229-5178


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A Case of Subcutaneous Thumb Tumor

A 58-year-old man presented with a 2-year history of a painless subcutaneous mass on the right thumb [Figure 1a]. The tumor had gradually increased in size and there was no preceding history of trauma. Physical examination revealed a solitary tumor on the thumb tip underneath indurate, pink skin of 1 cm size. A radiograph of the affected part revealed no abnormality. Histological examination revealed a mass composed of spindle-shaped cells [Figure 1b and c].
Figure 1

(a) Pink-colored subcutaneous nodule. (b) Well-circumscribed ovoid tumor (H and E, x40). (c) Verocay body with horizontal rows of palisading nuclei separated by areas of acellular pink basement membrane-like material (Hematoxylin–eosin stain; 100 × original magnification)

(a) Pink-colored subcutaneous nodule. (b) Well-circumscribed ovoid tumor (H and E, x40). (c) Verocay body with horizontal rows of palisading nuclei separated by areas of acellular pink basement membrane-like material (Hematoxylineosin stain; 100 × original magnification)

Answer

Schwannoma

Discussion

Schwannomas are benign, slow-growing tumors of neural tissue that arise from Schwann cells.[1] It is the most common tumor of the peripheral nerves; most of them are located intracranially or intraspinally, and less than 1% occurs in the hand.[2] They begin to appear between 30 and 60 years of age.[3] Presentation is as a subcutaneous mass with a fibrous capsule. Sometimes, pain is the chief complaint. Clinically, it may be difficult to differentiate from neurofibromas, giant cell tumors, ganglions, lipomas, periungual fibroma, digital fibrokeratoma, glomus tumors, and exostoses. Histological examination revealed a biphasic pattern, cellular areas of closely packed spindle cells with nuclear palisading [Figure 1b and c] (Verocay bodies) termed Antoni type A, and less cellular areas with a myxoid matrix, termed Antoni type B.[4] Histological variants are ancient, cellular, plexiform, melanotic, epithelioid, and pacinian. Surgical excision is curative and recurrence is rare.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.
  4 in total

1.  Schwannoma of a digit.

Authors:  Natsuko Ishida; Daisuke Watanabe; Kazuhisa Yokoo; Yasuhiko Tamada; Yoshinari Matsumoto
Journal:  Eur J Dermatol       Date:  2006 Jul-Aug       Impact factor: 3.328

2.  Schwannoma of the hand in an infant: case report.

Authors:  Ian C Sando; Shimpei Ono; Kevin C Chung
Journal:  J Hand Surg Am       Date:  2012-08-31       Impact factor: 2.230

3.  Schwannomas of the upper extremity: diagnosis and treatment.

Authors:  Roberto Adani; Alessio Baccarani; Enrico Guidi; Luigi Tarallo
Journal:  Chir Organi Mov       Date:  2008-07-08

4.  A consecutive 7-year series of 1331 benign soft tissue tumours. Clinicopathologic data. Comparison with sarcomas.

Authors:  O Myhre-Jensen
Journal:  Acta Orthop Scand       Date:  1981-06
  4 in total

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