<!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v2.3 20070202//EN" "journalpublishing.dtd">
<article article-type="case-report" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML">
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Our Dermatol Online</journal-id>
<journal-title>Our Dermatol Online</journal-title>
<issn pub-type="epub">2081-9390</issn>
<publisher>
<publisher-name>Our Dermatology Online</publisher-name>
<publisher-loc>Poland</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">OURD-7-403</article-id>
<article-id pub-id-type="doi">10.7241/ourd.20164.110</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Bazex-syndrome with esophageal cancer</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Boldt</surname>
<given-names>Sebastian</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wollina</surname>
<given-names>Uwe</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
<xref ref-type="corresp" rid="cor1"/>
</contrib>
</contrib-group>
<aff id="aff1"><italic>Department of Dermatology and Allergology, Academic Teaching Hospital Dresden-Friedrichstadt, 01067 Dresden, Germany</italic></aff>
<author-notes>
<corresp id="cor1">
<bold>Corresponding author:</bold> Prof. Uwe Wollina, E-mail: <email xlink:href="wollina-uw@khdf.de">wollina-uw@khdf.de</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<year>2016</year>
</pub-date>
<volume>7</volume>
<issue>4</issue>
<fpage>403</fpage>
<lpage>405</lpage>
<history>
<date date-type="received"><day>09</day><month>04</month><year>2016</year></date>
<date date-type="accepted"><day>13</day><month>06</month><year>2016</year></date>
</history>
<permissions>
<copyright-statement>Copyright: &#x000a9; Our Dermatol Online 4</copyright-statement>
<copyright-year>2016</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-sa/3.0">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p>
</license>
</permissions>
<abstract>
<p>Skin diseases can be a first sign of internal malignancies. Acrokeratosis neoplastica or Bazex-syndrome is a rare obligatory paraneoplastic dermatosis. We report on a 51-year-old male patient who complaint about reduced physical working capacity, swelling of fingers and toes. He presented with non-itching violaceous erythemato-squamous lesions on nose, hands and feet. On examination we observed onychomadesis of finger nails. Thoracic computerized tomography disclosed a tumor mass in the distal esophagus. Endosonography with trans-esophageal fine-needle biopsy confirmed the diagnosis of esophageal squamous cell carcinoma. The knowledge of cutaneous paraneoplasias allows an earlier diagnosis of internal malignancies.</p>
</abstract>
<kwd-group>
<kwd>Paraneoplastic skin disease</kwd>
<kwd>Acrokeratosis neoplastica</kwd>
<kwd>Bazex-syndrome</kwd>
<kwd>Esophageal squamous cell carcinoma</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="sec1-1" sec-type="intro">
<title>INTRODUCTION</title>
<p>Human skin can be a mirror for internal disorders including malignancies. The cutaneous signs and symptoms may often precede the development of clinical tumor-associated complaints. The so-called cutaneous paraneoplasias will help to identify internal malignancies earlier [<xref ref-type="bibr" rid="ref1">1</xref>].</p>
<p>We differentiate cutaneous paraneoplasias in facultative such as erythema gyratum repens and obligate such as acrokeratosis paraneoplastica. The latter is also known as Bazex-syndrome. Bazex et al. described the syndrome in 1965 in a patient with a larynx tumor [<xref ref-type="bibr" rid="ref2">2</xref>]. In 75&#x0025; of cases Bazex-syndrome develops before the diagnosis of malignancies. Its diagnosis should lead to a detailed search for cancer [<xref ref-type="bibr" rid="ref3">3</xref>]. Associated tumors are mainly found in pharynx and larynx (48.6&#x0025;), lungs (17.7&#x0025;), and esophagus (10.6&#x0025;) [<xref ref-type="bibr" rid="ref2">2</xref>].</p>
<p>Here we report a 51-year-old male patient with Bazex-syndrome and esophageal squamous cell carcinoma (SCC).</p>
</sec>
<sec id="sec1-2" sec-type="cases">
<title>CASE REPORT</title>
<p>A 51-year-old male patient was referred from the rheumatologist for diagnosis of cutaneous lesions, that developed during the last 5 months. He had a medical history for arterial hypertension, chronic obstructive pulmonary disease (COPD), and smoking. His medical family history was unremarkable.</p>
<p>He noticed a reduced physical working capacity. The patient also complaint about swelling of fingers and toes. He had neither arthritis nor arthralgia or morning stiffness, no dysphagia. Skin of nose, hands and feet presented with violaceous erythema and scaling (<xref ref-type="fig" rid="F1">Fig. 1a</xref> and <xref ref-type="fig" rid="F1">1b</xref>). The lesions were not itching. Fingernails demonstrated onychomadesis (<xref ref-type="fig" rid="F2">Fig. 2</xref>).</p>
<fig id="F1">
<label>Figure 1</label>
<caption>
<p>Acrokeratosis neoplastica (Bazex-syndrome). Violaceous erythemato-squamous lesions resembling psoriasis. (a) Nose. (b) Feet with edematous swelling of toes.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-7-403-g001.tif"/>
</fig>
<fig id="F2">
<label>Figure 2</label>
<caption>
<p>Hand in Bazex-syndrome with psoriasis-like cutaneous lesions and onychomadesis of nails.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-7-403-g002.tif"/>
</fig>
<p>Laboratory investigations were unremarkable for routine lab, antinuclear antibodies, antibodies against extractable nuclear antigens, citrullin, rheumatoid factor. Neither cryoglobulins nor cold agglutinins were detected. Immune fixation was normal. Only minor iron-deficient anemia was noted.</p>
<p>He had no signs of vascular disorders.</p>
<p>Computerized tomography (CT) disclosed a tumor mass of the esophagus measuring about 36 x 39 mm (Figs. <xref ref-type="fig" rid="F3">3a</xref> and <xref ref-type="fig" rid="F3">3b</xref>). Endosonography with trans-esophageal fine-needle puncture was performed to obtain tissue for histopathology. The diagnosis of a squamous cell carcinoma (SCC) of the esophagus was confirmed.</p>
<fig id="F3">
<label>Figure 3</label>
<caption>
<p>Computerized tomography of esophageal squamous cell carcinoma. (a) Transaxial view and (b) sagittal view. The arrow in (a) points to the tumor.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-7-403-g003.tif"/>
</fig>
<p>Palliative chemotherapy or radiotherapy were suggested since the tumor could no longer been resected surgically.</p>
</sec>
<sec id="sec1-3" sec-type="discussion">
<title>DISCUSSION</title>
<p>Acrokeratosis neoplastica or Bazex-syndrome is a rare obligate paraneoplasia. The typical patient is older than 50 years of age. There is a male predominance. Tumors of upper airways and digestive tract are on top of malignancies associated with Bazex-syndrome [<xref ref-type="bibr" rid="ref2">2</xref>-<xref ref-type="bibr" rid="ref7">7</xref>]. Cutaneous symptoms resemble psoriasis with bluish or violaceous erythema and scaling, onychodystropy, and/or keratoderma. There is usually no pruritus. Typically, these lesions occur symmetrical on acral body parts like ears, nose, hands and feet [<xref ref-type="bibr" rid="ref2">2</xref>-<xref ref-type="bibr" rid="ref5">5</xref>]. Uncommon manifestations include flexural Bazex-syndrome, which was seen in a patient with tonsillar adenocarcinoma [<xref ref-type="bibr" rid="ref6">6</xref>], or genital involvement [<xref ref-type="bibr" rid="ref7">7</xref>]. Histopathology of cutaneous lesions is non-specific psoriasiform.</p>
<p>Our patient demonstrated onychomadesis of finger nails like the patient of Graves et al [<xref ref-type="bibr" rid="ref7">7</xref>]. Other nail findings are subungual keratosis, yellowish discoloration, ridging, and onycholysis [<xref ref-type="bibr" rid="ref2">2</xref>].</p>
<p>We detected an associated esophageal SCC. The patient had not reported any symptoms. Due to the size and topography of the tumor curative surgery was, however, no longer possible. Radiotherapy with cumulative doses between 50 to 70 Gy leads to 5-year survival rates of 23&#x0025; [<xref ref-type="bibr" rid="ref8">8</xref>].</p>
<p>In contrast to tumor therapy, treatment of cutaneous Bazex symptoms is of minor importance. Moisturizers and topical corticosteroids may be used but are not very effective. On the other hand, Bazex-syndrome disappears in more than 90&#x0025; after successful tumor therapy [<xref ref-type="bibr" rid="ref9">9</xref>] but in other cases Bazex-syndrome persists due to unknown reasons [<xref ref-type="bibr" rid="ref10">10</xref>].</p>
</sec>
</body>
<back>
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<fn-group>
<fn fn-type="supported-by">
<p><bold>Source of Support:</bold> Nil</p>
</fn>
<fn fn-type="conflict">
<p><bold>Conflict of Interest:</bold> None declared.</p>
</fn>
</fn-group>
</back>
</article>