<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">CRCM</journal-id><journal-title-group><journal-title>Case Reports in Clinical Medicine</journal-title></journal-title-group><issn pub-type="epub">2325-7075</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/crcm.2015.49063</article-id><article-id pub-id-type="publisher-id">CRCM-59846</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Basal Cell Carcinoma Arising from a Follicular Hybrid Cyst
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>akayuki</surname><given-names>Aizu</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Takahide</surname><given-names>Kaneko</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Noriko</surname><given-names>Takiyoshi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Satoko</surname><given-names>Minakawa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ayumi</surname><given-names>Korekawa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hajime</surname><given-names>Nakano</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Daisuke</surname><given-names>Sawamura</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Dermatology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>derma@hirosaki-u.ac.jp(DS)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>07</day><month>09</month><year>2015</year></pub-date><volume>04</volume><issue>09</issue><fpage>317</fpage><lpage>320</lpage><history><date date-type="received"><day>4</day>	<month>August</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>20</month>	<year>September</year>	</date><date date-type="accepted"><day>23</day>	<month>September</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Malignant tumors arising from follicular cysts are rare. Herein, we report of a 62-year-old Japanese woman with a slowly growing tumor, 22 &#215; 20 mm in size, located on her nose for 2 years. Histopathological examination of the surgically excised tumor showed that the tumor cells were basaloid and formed peripheral palisading patterns. The tumor contained a cystic structure in its center, and the cyst wall was lined with stratified epithelium with or without keratohyalin granules. Based on these findings, a diagnosis of basal cell carcinoma arising from a follicular hybrid cyst was made. To our knowledge, this is the first case of basal cell carcinoma originating from a follicular hybrid cyst. A review of previous reports of basal cell carcinoma from a follicular cyst indicated that the majority of previous cysts were located on the face, and that the lesions had been present for a relatively long time. The present case showed typical clinical findings and followed a regular course. Malignant transformation may be a rare event, but it can occur in a follicular cyst, so cysts and suspected cysts, especially those found on the face and those persisting for relatively long time, should always be subjected to histological examination.
 
</p></abstract><kwd-group><kwd>Epidermoid Cysts</kwd><kwd> Trichilemmal Cyst</kwd><kwd> Malignant Transformation</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>There are two types of follicular cysts: epidermoid and trichilemmal. Epidermoid cysts produce keratohyalin, which forms a horny material resembling the epidermis. Trichilemmal cysts are characterized by abrupt keratinization without keratohyalin granules. Furthermore, there are hybrid cysts, which are combinatory keratinous cysts with both epidermoid and trichilemmal zones that are separated by an abrupt transition [<xref ref-type="bibr" rid="scirp.59846-ref1">1</xref>] . Malignant tumors arising from follicular cysts are rare. Herein, we report a case of basal cell carcinoma arising from a follicular hybrid cyst of the skin.</p></sec><sec id="s2"><title>2. Case Report</title><p>A 62-year-old Japanese woman with a slowly growing tumor on her nose for 2 years was referred to our department for evaluation. Physical examination revealed an erythematous, irregularly pigmented, 22- &#215; 20-mm dermal tumor on the left dorsum of her nose (<xref ref-type="fig" rid="fig1">Figure 1</xref>(a)). Dermoscopy of the tumor showed multiple blue-gray ovoid nests and arborizing vessels (<xref ref-type="fig" rid="fig1">Figure 1</xref>(b)), and ultrasonography of the tumor demonstrated a low echoic area indicating a cystic structure (<xref ref-type="fig" rid="fig1">Figure 1</xref>(c)).</p><p>With a provisional diagnosis of basal cell carcinoma, a punch biopsy was performed under local anesthesia. The specimen showed various-sized islands of uniform basaloid cells showing peripheral palisading patterns (<xref ref-type="fig" rid="fig2">Figure 2</xref>(a)); diagnosis was confirmed as basal cell carcinoma.</p><p>Surgical excision of the tumor was performed. Histopathological examination showed that the whole tumor extended from the upper dermis to the subcutaneous tissue (<xref ref-type="fig" rid="fig2">Figure 2</xref>(b)). The tumor cells were basaloid and formed peripheral palisading patterns. The tumor contained a cystic structure in its center and the tumor cell nests were not separated from their associated stroma. The cyst wall was lined with stratified epithelium with or without keratohyalin granules (<xref ref-type="fig" rid="fig2">Figure 2</xref>(c) and <xref ref-type="fig" rid="fig2">Figure 2</xref>(d)). A portion of the wall was replaced by basaloid cells without stratified epithelium. Immunohistochemical staining showed that the tumor cells were positive for Ber-EP4. Based on these findings, basal cell carcinoma arising in a follicular hybrid cyst was diagnosed.</p></sec><sec id="s3"><title>3. Discussion</title><p>Cysts of the skin are very common, and the most frequent cutaneous cysts are follicular cysts, the walls of which are lined by stratified squamous epithelia. There are two types of follicular cysts: epidermoid and trichilemmal. Epidermoid cysts are lined by a keratinized epithelium with a distinct granular layer, and the site of origin is thought to be the infundibular portion of the hair follicle. On the other hand, trichilemmal cysts originate from the outer hair root sheath. The wall of the cyst consists of stratified squamous epithelium that has a palisaded outer layer, and the inner layer does not have a granular layer. The hybrid cyst is a combination of epidermoid and trichilemmal cysts [<xref ref-type="bibr" rid="scirp.59846-ref1">1</xref>] .</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Clinical, dermoscopic, and ultrasonographic findings. (a) An irregularly pigmented erythematous dermal tumor on the left dorsum of the nose, 22 &#215; 20 mm in size; (b) Dermoscopy showed multiple blue-gray ovoid nests and arborizing vessels; (c) Ultrasonography demonstrated low echoic area in the center of the tumor indicating a cystic structure</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/4-2770578x6.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Histological findings. (a) The biopsy specimen showed various-sized islands of uniform basaloid cells showing peripheral palisading patterns. HE staining, 40&#215;. (b) The whole tumor encompassed the region from the upper dermis to the subcutaneous tissue. The tumor cells were basaloid and formed peripheral palisading patterns. The tumor consisted of a cystic structure in its center; the tumor cell nests were not separated from their associated stroma. HE staining, 4&#215;. (c) and (d) The cyst wall was lined with stratified epithelium with (c) or without (d) keratohyalin granules. HE staing, 200&#215;</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/4-2770578x7.png"/></fig><p>Malignant tumors arising from follicular cysts are rare. Cameron and Hilsinger reported that only one squamous cell carcinoma was found among 2246 cases of epidermoid cysts, and there were no cases of basal cell carcinoma [<xref ref-type="bibr" rid="scirp.59846-ref2">2</xref>] . Delacretaz reviewed malignant tumors arising from follicular cysts and added a case of his own [<xref ref-type="bibr" rid="scirp.59846-ref3">3</xref>] . Among these cases, 51 were squamous cell carcinomas, 18 were basal cell carcinomas, 3 were baso- squamous cell carcinomas, and the remaining 5 were not specified. Focusing on basal cell carcinoma cases arising from follicular cysts, 8 were from an epidermoid cyst and 3 were from a trichilemmal cyst, and in the remaining 7 cases, the cyst types were not specified. Tsujita-Kyotoku et al. reviewed 13 Japanese cases of basal cell carcinoma from follicular cysts [<xref ref-type="bibr" rid="scirp.59846-ref4">4</xref>] . Clinically, most of the cysts were located on the face and ranged from 0.7 to 6.0 cm in diameter. The lesions had been present for a relatively long time, ranging from 1.5 months to 56 years. The present case was observed in a 62-year-old woman; her tumor was 22 &#215; 20 mm in size, and it had been growing slowly for 2 years on her nose. Thus, the present case showed typical clinical findings and followed a typical course. Also, there was two cases of basal cell carcinoma from epidermoid cyst form Japan [<xref ref-type="bibr" rid="scirp.59846-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.59846-ref6">6</xref>] . Tsujita-Kyotoku et al. also determined that basal cell caricinoma was shown to arise histologically from an epidermoid cyst in 8 patients, from a trichilemmal cyst in 3, and from an atheroma (unknown) in 2 [<xref ref-type="bibr" rid="scirp.59846-ref4">4</xref>] ; there was no hybrid cyst in the 13 previously described cases. As far as we know, there are no previous reports of basal cell carcinoma originating from a follicular hybrid cyst.</p><p>Basal cell carcinoma is the most common malignant tumor in the dermatological field. However, squamous cell carcinoma is the most common among malignant tumors arising from a follicular cyst [<xref ref-type="bibr" rid="scirp.59846-ref3">3</xref>] . Sun exposure is the most important environmental cause of basal cell carcinoma. Much less ultraviolet right reaches a follicular cyst than other sun-exposed areas; this may explain the inversion of the frequencies of basal and squamous cell carcinomas in follicular cysts.</p><p>Follicular cysts are extremely common skin tumors; as a result, their excision and histological examination is sometimes omitted in clinical practice. Malignant transformation may be a rare event, but it can definitely occur in follicular cysts, so cysts and suspected cysts, especially those occurring on the face and those persisting for a relatively long time, should always be subjected to histological examination.</p></sec><sec id="s4"><title>Cite this paper</title><p>TakayukiAizu,TakahideKaneko,NorikoTakiyoshi,SatokoMinakawa,AyumiKorekawa,HajimeNakano,DaisukeSawamura, (2015) Basal Cell Carcinoma Arising from a Follicular Hybrid Cyst. Case Reports in Clinical Medicine,04,317-320. doi: 10.4236/crcm.2015.49063</p></sec><sec id="s5"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.59846-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Brownstein, M.H. (1983) Hybrid Cyst: A Combined Epidermoid and Trichilemmal Cyst. Journal of the American Academy of Dermatology, 9, 872-875. http://www.ncbi.nlm.nih.gov/pubmed/6643785 http://dx.doi.org/10.1016/s0190-9622(83)70201-x</mixed-citation></ref><ref id="scirp.59846-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Cameron, D.S. and Hilsinger Jr., R.L. (2003) Squamous Cell Carcinoma in an Epidermal Inclusion Cyst: Case Report. Otolaryngology—Head and Neck Surgery, 129, 141-143. http://dx.doi.org/10.1016/S0194-5998(03)00466-2</mixed-citation></ref><ref id="scirp.59846-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Delacrétaz, J. 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