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JAMA Clinical Challenge |

Cutaneous Nodule in a Young Man FREE

Jianjun Qiao, MD, PhD; Hong Fang, MD
[+] Author Affiliations

Author Affiliations: Department of Dermatology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.


JAMA Clinical Challenge Section Editor: Huan J. Chang, MD, Contributing Editor. We encourage authors to submit papers for consideration as a JAMA Clinical Challenge. Please contact Dr Chang at tina.chang@jamanetwork.org

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JAMA. 2012;308(8):812-813. doi:10.1001/jama.2012.9637.
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A 21-year-old male student presents with a nodule on his chest that has been progressively enlarging over 1 month. He also has a 1-month history of upper abdominal pain associated with diarrhea but without fever or chills. He was diagnosed with acute gastroenteritis and treated with oral omeprazole and ofloxacin without relief. He has lost 5 kg during the past half year. He denies any history of chronic illness or family history of cancer. Physical examination reveals left supraclavicular and cervical lymphadenopathy. A solitary asymptomatic, nontender, and indurated nodule is found on his chest (Figure 1). Gastrointestinal endoscopy shows multiple ulcers on the gastric fundus and gastric corpus.

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Figure 1. Solitary nodule on the chest.
Grahic Jump Location

  • A. Consult a surgeon for excision of the nodule

  • B. Do nothing; the nodule will resolve over time

  • C. Inject corticosteroids intralesionally

  • D. Obtain a biopsy of the nodule

Cutaneous metastasis of gastric adenocarcinoma

D. Obtain a biopsy of the nodule

The key clinical feature to recognize in this case is the rapidly growing asymptomatic nodule associated with gastrointestinal symptoms. Although cutaneous metastases of gastric adenomas are uncommon especially in younger persons, a rapidly growing asymptomatic skin nodule of undetermined causes should be biopsied. If cutaneous metastasis is diagnosed, the origin of metastases should be found.

Virtually any tumor of the visceral organs can metastasize to the skin. However, cutaneous metastases are uncommon, with a reported frequency of 0.7% to 10.4%.15 Metastases are usually a late manifestation of widely disseminated disease, but occasionally they may be the first indication of an undiagnosed internal malignancy.23,6 Cutaneous metastases usually originate from the breast, lungs, colon, rectum, ovary, head and neck, or kidney.23

Malignant cutaneous lesions indicative of systemic cancer most commonly occur as asymptomatic multiple nodules (46.6%), single nodules (37.7%), plaques or erythematous patches (9.4%), and ulcers (6.5%).6 Metastases typically present with relatively sudden onset and rapid growth.1,67 Skin metastases may be isolated or associated with metastases at multiple sites.3,8

Gastric carcinoma is usually detected after the fifth decade of life9 and is rare in adults younger than 30 years.9 The most common metastatic sites from gastric carcinoma are liver, intra-abdominal lymph nodes, ovary, and peritoneal cavity.3,67 Gastric carcinoma presents as skin metastasis 6.4% to 7.8% of the time.2,8 The lesions of cutaneous metastases of gastric carcinoma are usually located on the abdominal wall or near the lymph nodes2,8 and are similar to cutaneous metastases of other malignancies.

Lesions of cutaneous metastases may be clinically indistinguishable from benign lesions, such as hemangiomas, epidermal cysts, pyogenic granulomas, or neurofibromas.12,7 Diagnosis depends on histological evaluation combined with immunohistochemical staining.8 Histologically, cutaneous metastases usually show features consistent with the underlying primary malignancy. However, metastases may exhibit less differentiation and be more anaplastic.2,7 The survival rate of patients with cutaneous metastases from internal malignancies is usually low.67 The median duration of survival after cutaneous metastases from gastric carcinoma is not known.

In this patient, a biopsy revealed infiltrating neoplastic cells scattered or clustered in the dermis. Some neoplastic cells appeared as signet ring cells (Figure 2A). Immature lumens of glands consistent with neoplastic cells were found in the deep dermis (Figure 2B). There was a narrow layer beneath the epidermis that is not infiltrated by atypical cells distributed in the deep dermis. Immunohistochemically, the signet ring cells were positive for carcinoembryonic antigen, epithelial membrane antigen, and CK20 and negative for markers of CD3, CD4, CD8, CD30, and gross cystic disease fluid protein 15 (GCDFP-15). Staining with Ki-67 indicated prominent proliferative activity. Mucin stained positively in the metastatic cells with Alcian blue. These pathological studies indicated a diagnosis of secondary signet ring cell adenocarcinoma and suggested digestive tractorigin. Pathology of biopsy specimens from ulcers in the stomach was compatible with a gastric signet ring cell adenocarcinoma. Abdominal computed tomography detected many metastatic nodules in mesentery, hepatic hilar region, and retroperitoneal lymph nodes. In view of the metastases, surgical intervention would be noncurative. The patient received chemotherapy with oxaliplatin (day 1) and S-1 (egafur, gimestat, and oteracil potassium) (days 1 to 7). His symptoms improved and the size of the nodule reduced after 2 weeks of the chemotherapy.

Place holder to copy figure label and caption
Figure 2. Histology of the nodule. A, Some neoplastic cells appeared as signet ring cells. B, Immature lumens of glands (both panels: hematoxylin-eosin, original magnification ×400).
Grahic Jump Location

Corresponding Author: Hong Fang, MD, Department of Dermatology, The First Affiliated Hospital, College of Medicine, Zhejiang University, No. 79, Qingchun Road, Hangzhou, 310003 Zhejiang Province, People's Republic of China (fanghongzy@sina.com).

Conflict of Interest Disclosures: Both authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest and none were reported.

Additional Contributions: We thank the patient for providing permission to publish his information.

Chopra R, Chhabra S, Samra SG,  et al.  Cutaneous metastases of internal malignancies.  Indian J Dermatol Venereol Leprol. 2010;76(2):125-131
PubMed   |  Link to Article
Lookingbill DP, Spangler N, Helm KF. Cutaneous metastases in patients with metastatic carcinoma: a retrospective study of 4020 patients.  J Am Acad Dermatol. 1993;29(2 pt 1):228-236
PubMed
Sariya D, Ruth K, Adams-McDonnell R,  et al.  Clinicopathologic correlation of cutaneous metastases.  Arch Dermatol. 2007;143(5):613-620
PubMed
Nashan D, Müller ML, Braun-Falco M,  et al.  Cutaneous metastases of visceral tumours: a review.  J Cancer Res Clin Oncol. 2009;135(1):1-14
PubMed
Hu SC, Chen GS, Wu CS,  et al.  Rates of cutaneous metastases from different internal malignancies: experience from a Taiwanese medical center.  J Am Acad Dermatol. 2009;60(3):379-387
PubMed
Hu SC, Chen GS, Lu YW,  et al.  Cutaneous metastases from different internal malignancies.  J Eur Acad Dermatol Venereol. 2008;22(6):735-740
PubMed
Nashan D, Meiss F, Braun-Falco M, Reichenberger S. Cutaneous metastases from internal malignancies.  Dermatol Ther. 2010;23(6):567-580
PubMed
Saeed S, Keehn CA, Morgan MB. Cutaneous metastasis: a clinical, pathological, and immunohistochemical appraisal.  J Cutan Pathol. 2004;31(6):419-430
PubMed
Torpy JM. Stomach cancer [JAMA Patient Page].  JAMA. 2010;303(17):1771
PubMed

Figures

Place holder to copy figure label and caption
Figure 1. Solitary nodule on the chest.
Grahic Jump Location
Place holder to copy figure label and caption
Figure 2. Histology of the nodule. A, Some neoplastic cells appeared as signet ring cells. B, Immature lumens of glands (both panels: hematoxylin-eosin, original magnification ×400).
Grahic Jump Location

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References

Chopra R, Chhabra S, Samra SG,  et al.  Cutaneous metastases of internal malignancies.  Indian J Dermatol Venereol Leprol. 2010;76(2):125-131
PubMed   |  Link to Article
Lookingbill DP, Spangler N, Helm KF. Cutaneous metastases in patients with metastatic carcinoma: a retrospective study of 4020 patients.  J Am Acad Dermatol. 1993;29(2 pt 1):228-236
PubMed
Sariya D, Ruth K, Adams-McDonnell R,  et al.  Clinicopathologic correlation of cutaneous metastases.  Arch Dermatol. 2007;143(5):613-620
PubMed
Nashan D, Müller ML, Braun-Falco M,  et al.  Cutaneous metastases of visceral tumours: a review.  J Cancer Res Clin Oncol. 2009;135(1):1-14
PubMed
Hu SC, Chen GS, Wu CS,  et al.  Rates of cutaneous metastases from different internal malignancies: experience from a Taiwanese medical center.  J Am Acad Dermatol. 2009;60(3):379-387
PubMed
Hu SC, Chen GS, Lu YW,  et al.  Cutaneous metastases from different internal malignancies.  J Eur Acad Dermatol Venereol. 2008;22(6):735-740
PubMed
Nashan D, Meiss F, Braun-Falco M, Reichenberger S. Cutaneous metastases from internal malignancies.  Dermatol Ther. 2010;23(6):567-580
PubMed
Saeed S, Keehn CA, Morgan MB. Cutaneous metastasis: a clinical, pathological, and immunohistochemical appraisal.  J Cutan Pathol. 2004;31(6):419-430
PubMed
Torpy JM. Stomach cancer [JAMA Patient Page].  JAMA. 2010;303(17):1771
PubMed
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