A rapidly growing crusted nodule on the lip

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A rapidly growing crusted nodule on the lip
Author(s)
Paul J. Wirth
Thomas N. Helm, MD

A 76-year-old man presented with a rapidly growing, indurated, crusted nodule on his lower lip (Figure 1). This combination—a rapidly growing nodule on a sun-exposed surface in an older patient—pointed to a diagnosis of squamous cell carcinoma, and biopsy study of the affected area confirmed this diagnosis (Figure 2). Clinical examination, computed tomography, and ultrasonography of the neck revealed no lymph node involvement; the tumor was staged as T2N0M0. Mohs microscopically controlled surgery was performed to remove the tumor with clear margins, and the patient has done well.

DIFFERENTIAL DIAGNOSIS

Figure 1. The lesion was crusted and indurated. The view on the right shows the markings for the planned surgical removal.

Malignant melanoma, Merkel cell carcinoma, and deep fungal infection can also cause a rapidly growing crusted nodule on the lower lip, but this typically is not an initial presentation for these conditions.

Malignant melanoma

Figure 2. Histologic examination (left) revealed keratinocytes with enlarged and pleomorphic nuclei (black arrow). Atypical mitotic figures were also noted (red arrow) (hematoxylin and eosin, × 200). The high-power view (right) also shows enlarged and pleomorphic nuclei (black arrow) and atypical mitotic figures (red arrow) (hematoxylin and eosin, × 400).

Malignant melanoma should be considered for any rapidly growing cutaneous tumor, especially on sun-damaged skin. Most melanoma lesions have variations in pigment and may contain shades of blue, brown, red, pink, and white. Amelanotic melanomas may mimic squamous cell carcinomas, but the histologic features of atypical keratinocytes in this patient ruled out that diagnosis. Biopsy of amelanotic melanoma reveals nests of melanocytes, usually associated with an in situ component in the overlying epithelium.

Merkel cell carcinoma

Merkel cell carcinoma can mimic squamous cell carcinoma or can even arise in association with squamous cell carcinoma. Histologic examination allows for differentiation. In difficult cases, cytokeratin staining with cytokeratin 20 and CAM 5.2 can clarify the diagnosis, because Merkel cell carcinomas exhibit a characteristic paranuclear dot-like pattern not evident in squamous cell carcinoma.

Deep fungal infection

Colonization by Candida organisms was noted within the overlying crust in this patient’s lesion, but fungal organisms were not noted in the epidermis or dermis. Pseudoepitheliomatous hyperplasia can be prominent in deep fungal infection, but the marked cytologic atypia in this case excluded deep fungal infection.

Mucosal neuroma

Mucosal neuromas are typically smooth-surfaced, soft lesions on the lip. They may be associated with multiple endocrine neoplasia syndromes. Biopsy study reveals that they are composed of delicate spindle cells that lack atypia.

SQUAMOUS CELL CARCINOMA

Squamous cell carcinoma is one of the most common types of nonmelanoma skin cancer and is associated with increased sun exposure and light skin pigmentation.1 Unlike basal cell carcinoma, squamous cell carcinoma has a considerable potential to metastasize.2–4 The current cancer staging manual of the American Joint Commission on Cancer refects recent evidence-based information on staging and prognosis.5–7 Squamous cell carcinoma of the lip carries an increased risk of metastasis,8 and an increase in the number or the size of involved lymph nodes carries a worse prognosis.9 The lower lip is most commonly involved because of increased sun exposure. The most common route for the spread of squamous cell carcinoma of the head and neck is via lymphatics, so careful evaluation of the head and neck is indicated.10

STAGING OUR PATIENT’S LESION

Current staging of cutaneous squamous cell carcinoma takes into account a variety of different features. Our patient’s tumor was not associated with invasion of the maxilla, mandible, orbit, or temporal bone. This alone would have qualified the tumor as a T1 lesion, but its size of 3 cm indicated a higher risk and qualified it as a T2 lesion.

The histologic features of our patient’s lesion also indicate higher risk according to the current staging system.5 The Breslow thickness on histologic examination (measured from the granular cell layer of the epidermis to the deepest portion of the tumor) was 4 mm and the Clark’s level was IV (extension to the reticular dermis). The high-risk features and the location on the lip warrant a classification as T2 and carry a worse prognosis.

Wedge excision of the lower lip and Mohs surgery are accepted treatment options. The patient chose Mohs surgery and has done well, with excellent cosmetic and functional outcome. Radiation therapy can be useful as an adjuvant when lymph nodes are involved,11 but this was not necessary in our patient. Careful long-term follow up is warranted, as these patients are at higher risk of developing other, separate tumors.

References
  1. Schwartz RA. Squamous cell carcinoma. In:Schwartz RA, editor. Skin Cancer: Recognition and Management, 2nd ed. Malden, MA: Blackwell Publishing; 2008:47–65.
  2. D’Souza J, Clark J. Management of the neck in metastatic cutaneous squamous cell carcinoma of the head and neck. Curr Opin Otolaryngol Head Neck Surg 2011; 19:99–105.
  3. Zbar RI, Canady JW. MOC-PSSM CME article: Nonmelanoma facial skin malignancy. Plast Reconstr Surg 2008; 121(suppl 1):1–9.
  4. Morselli P, Masciotra L, Pinto V, Zollino I, Brunelli G, Carinci F. Clinical parameters in T1N0M0 lower lip squamous cell carcinoma. J Craniofac Surg 2007; 18:1079–1082.
  5. American Joint Commission on Cancer. Cancer Staging Manual. 7th ed. http://www.cancerstaging.org. Accessed February 3, 2013.
  6. Lardaro T, Shea SM, Sharfman W, Liégeois N, Sober AJ. Improvements in the staging of cutaneous squamous-cell carcinoma in the 7th edition of the AJCC Cancer Staging Manual. Ann Surg Oncol 2010; 17:1979–1980.
  7. Cutaneous squamous cell carcinoma and other cutaneous carcinomas. In:Edge SB, Byrd DR, Compton CC, Fritz AG, Greene FL, Trotti A, editors. AJCC Cancer Staging Manual. 7th ed. New York, NY: Springer; 2010:301–314.
  8. Frierson HF, Cooper PH. Prognostic factors in squamous cell carcinoma of the lower lip. Hum Pathol 1986; 17:346–354.
  9. Civantos FJ, Moffat FL, goodwin WJ. Lymphatic mapping and sentinel lymphadenectomy for 106 head and neck lesions: contrasts between oral cavity and cutaneous malignancy. Laryngoscope 2006; 112(3 Pt 2 suppl 109):1–15.
  10. Rowe De, Carroll RJ, Day CL. Prognostic factors for local recurrence, metastasis, and survival rates in squamous cell carcinoma of the skin, ear, and lip. Implications for treatment modality selection. J Am Acad Dermatol 1992; 26:976–990.
  11. Veness MJ, Palme CE, Smith M, Cakir B, Morgan GJ, Kalnins I. Cutaneous head and neck squamous cell carcinoma metastatic to cervical lymph nodes (nonparotid): a better outcome with surgery and adjuvant radiotherapy. Laryngoscope 2003; 113:1827–1833.
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Paul J. Wirth
Department of Dermatopathology, Buffalo Medical Group, Williamsville, NY

Thomas N. Helm, MD
Department of Dermatopathology, Buffalo Medical Group, Williamsville, NY

Address: Thomas N. Helm, MD, Department of Dermatopathology, Buffalo Medical Group, 6225 Sheridan Drive, Suite 208, Building B, Williamsville, NY 14221; e-mail: [email protected]

Issue
Cleveland Clinic Journal of Medicine - 80(4)
Publications
Cleveland Clinic Journal of Medicine
Topics
Dermatology
Oncology
Page Number
222-224
Sections
The Clinical Picture
Author(s)
Paul J. Wirth
Thomas N. Helm, MD
Author(s)
Paul J. Wirth
Thomas N. Helm, MD
Author and Disclosure Information

Paul J. Wirth
Department of Dermatopathology, Buffalo Medical Group, Williamsville, NY

Thomas N. Helm, MD
Department of Dermatopathology, Buffalo Medical Group, Williamsville, NY

Address: Thomas N. Helm, MD, Department of Dermatopathology, Buffalo Medical Group, 6225 Sheridan Drive, Suite 208, Building B, Williamsville, NY 14221; e-mail: [email protected]

Author and Disclosure Information

Paul J. Wirth
Department of Dermatopathology, Buffalo Medical Group, Williamsville, NY

Thomas N. Helm, MD
Department of Dermatopathology, Buffalo Medical Group, Williamsville, NY

Address: Thomas N. Helm, MD, Department of Dermatopathology, Buffalo Medical Group, 6225 Sheridan Drive, Suite 208, Building B, Williamsville, NY 14221; e-mail: [email protected]

Article PDF
media_78903b4_222.pdf
Article PDF
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A 76-year-old man presented with a rapidly growing, indurated, crusted nodule on his lower lip (Figure 1). This combination—a rapidly growing nodule on a sun-exposed surface in an older patient—pointed to a diagnosis of squamous cell carcinoma, and biopsy study of the affected area confirmed this diagnosis (Figure 2). Clinical examination, computed tomography, and ultrasonography of the neck revealed no lymph node involvement; the tumor was staged as T2N0M0. Mohs microscopically controlled surgery was performed to remove the tumor with clear margins, and the patient has done well.

DIFFERENTIAL DIAGNOSIS

Figure 1. The lesion was crusted and indurated. The view on the right shows the markings for the planned surgical removal.

Malignant melanoma, Merkel cell carcinoma, and deep fungal infection can also cause a rapidly growing crusted nodule on the lower lip, but this typically is not an initial presentation for these conditions.

Malignant melanoma

Figure 2. Histologic examination (left) revealed keratinocytes with enlarged and pleomorphic nuclei (black arrow). Atypical mitotic figures were also noted (red arrow) (hematoxylin and eosin, × 200). The high-power view (right) also shows enlarged and pleomorphic nuclei (black arrow) and atypical mitotic figures (red arrow) (hematoxylin and eosin, × 400).

Malignant melanoma should be considered for any rapidly growing cutaneous tumor, especially on sun-damaged skin. Most melanoma lesions have variations in pigment and may contain shades of blue, brown, red, pink, and white. Amelanotic melanomas may mimic squamous cell carcinomas, but the histologic features of atypical keratinocytes in this patient ruled out that diagnosis. Biopsy of amelanotic melanoma reveals nests of melanocytes, usually associated with an in situ component in the overlying epithelium.

Merkel cell carcinoma

Merkel cell carcinoma can mimic squamous cell carcinoma or can even arise in association with squamous cell carcinoma. Histologic examination allows for differentiation. In difficult cases, cytokeratin staining with cytokeratin 20 and CAM 5.2 can clarify the diagnosis, because Merkel cell carcinomas exhibit a characteristic paranuclear dot-like pattern not evident in squamous cell carcinoma.

Deep fungal infection

Colonization by Candida organisms was noted within the overlying crust in this patient’s lesion, but fungal organisms were not noted in the epidermis or dermis. Pseudoepitheliomatous hyperplasia can be prominent in deep fungal infection, but the marked cytologic atypia in this case excluded deep fungal infection.

Mucosal neuroma

Mucosal neuromas are typically smooth-surfaced, soft lesions on the lip. They may be associated with multiple endocrine neoplasia syndromes. Biopsy study reveals that they are composed of delicate spindle cells that lack atypia.

SQUAMOUS CELL CARCINOMA

Squamous cell carcinoma is one of the most common types of nonmelanoma skin cancer and is associated with increased sun exposure and light skin pigmentation.1 Unlike basal cell carcinoma, squamous cell carcinoma has a considerable potential to metastasize.2–4 The current cancer staging manual of the American Joint Commission on Cancer refects recent evidence-based information on staging and prognosis.5–7 Squamous cell carcinoma of the lip carries an increased risk of metastasis,8 and an increase in the number or the size of involved lymph nodes carries a worse prognosis.9 The lower lip is most commonly involved because of increased sun exposure. The most common route for the spread of squamous cell carcinoma of the head and neck is via lymphatics, so careful evaluation of the head and neck is indicated.10

STAGING OUR PATIENT’S LESION

Current staging of cutaneous squamous cell carcinoma takes into account a variety of different features. Our patient’s tumor was not associated with invasion of the maxilla, mandible, orbit, or temporal bone. This alone would have qualified the tumor as a T1 lesion, but its size of 3 cm indicated a higher risk and qualified it as a T2 lesion.

The histologic features of our patient’s lesion also indicate higher risk according to the current staging system.5 The Breslow thickness on histologic examination (measured from the granular cell layer of the epidermis to the deepest portion of the tumor) was 4 mm and the Clark’s level was IV (extension to the reticular dermis). The high-risk features and the location on the lip warrant a classification as T2 and carry a worse prognosis.

Wedge excision of the lower lip and Mohs surgery are accepted treatment options. The patient chose Mohs surgery and has done well, with excellent cosmetic and functional outcome. Radiation therapy can be useful as an adjuvant when lymph nodes are involved,11 but this was not necessary in our patient. Careful long-term follow up is warranted, as these patients are at higher risk of developing other, separate tumors.

A 76-year-old man presented with a rapidly growing, indurated, crusted nodule on his lower lip (Figure 1). This combination—a rapidly growing nodule on a sun-exposed surface in an older patient—pointed to a diagnosis of squamous cell carcinoma, and biopsy study of the affected area confirmed this diagnosis (Figure 2). Clinical examination, computed tomography, and ultrasonography of the neck revealed no lymph node involvement; the tumor was staged as T2N0M0. Mohs microscopically controlled surgery was performed to remove the tumor with clear margins, and the patient has done well.

DIFFERENTIAL DIAGNOSIS

Figure 1. The lesion was crusted and indurated. The view on the right shows the markings for the planned surgical removal.

Malignant melanoma, Merkel cell carcinoma, and deep fungal infection can also cause a rapidly growing crusted nodule on the lower lip, but this typically is not an initial presentation for these conditions.

Malignant melanoma

Figure 2. Histologic examination (left) revealed keratinocytes with enlarged and pleomorphic nuclei (black arrow). Atypical mitotic figures were also noted (red arrow) (hematoxylin and eosin, × 200). The high-power view (right) also shows enlarged and pleomorphic nuclei (black arrow) and atypical mitotic figures (red arrow) (hematoxylin and eosin, × 400).

Malignant melanoma should be considered for any rapidly growing cutaneous tumor, especially on sun-damaged skin. Most melanoma lesions have variations in pigment and may contain shades of blue, brown, red, pink, and white. Amelanotic melanomas may mimic squamous cell carcinomas, but the histologic features of atypical keratinocytes in this patient ruled out that diagnosis. Biopsy of amelanotic melanoma reveals nests of melanocytes, usually associated with an in situ component in the overlying epithelium.

Merkel cell carcinoma

Merkel cell carcinoma can mimic squamous cell carcinoma or can even arise in association with squamous cell carcinoma. Histologic examination allows for differentiation. In difficult cases, cytokeratin staining with cytokeratin 20 and CAM 5.2 can clarify the diagnosis, because Merkel cell carcinomas exhibit a characteristic paranuclear dot-like pattern not evident in squamous cell carcinoma.

Deep fungal infection

Colonization by Candida organisms was noted within the overlying crust in this patient’s lesion, but fungal organisms were not noted in the epidermis or dermis. Pseudoepitheliomatous hyperplasia can be prominent in deep fungal infection, but the marked cytologic atypia in this case excluded deep fungal infection.

Mucosal neuroma

Mucosal neuromas are typically smooth-surfaced, soft lesions on the lip. They may be associated with multiple endocrine neoplasia syndromes. Biopsy study reveals that they are composed of delicate spindle cells that lack atypia.

SQUAMOUS CELL CARCINOMA

Squamous cell carcinoma is one of the most common types of nonmelanoma skin cancer and is associated with increased sun exposure and light skin pigmentation.1 Unlike basal cell carcinoma, squamous cell carcinoma has a considerable potential to metastasize.2–4 The current cancer staging manual of the American Joint Commission on Cancer refects recent evidence-based information on staging and prognosis.5–7 Squamous cell carcinoma of the lip carries an increased risk of metastasis,8 and an increase in the number or the size of involved lymph nodes carries a worse prognosis.9 The lower lip is most commonly involved because of increased sun exposure. The most common route for the spread of squamous cell carcinoma of the head and neck is via lymphatics, so careful evaluation of the head and neck is indicated.10

STAGING OUR PATIENT’S LESION

Current staging of cutaneous squamous cell carcinoma takes into account a variety of different features. Our patient’s tumor was not associated with invasion of the maxilla, mandible, orbit, or temporal bone. This alone would have qualified the tumor as a T1 lesion, but its size of 3 cm indicated a higher risk and qualified it as a T2 lesion.

The histologic features of our patient’s lesion also indicate higher risk according to the current staging system.5 The Breslow thickness on histologic examination (measured from the granular cell layer of the epidermis to the deepest portion of the tumor) was 4 mm and the Clark’s level was IV (extension to the reticular dermis). The high-risk features and the location on the lip warrant a classification as T2 and carry a worse prognosis.

Wedge excision of the lower lip and Mohs surgery are accepted treatment options. The patient chose Mohs surgery and has done well, with excellent cosmetic and functional outcome. Radiation therapy can be useful as an adjuvant when lymph nodes are involved,11 but this was not necessary in our patient. Careful long-term follow up is warranted, as these patients are at higher risk of developing other, separate tumors.

References
  1. Schwartz RA. Squamous cell carcinoma. In:Schwartz RA, editor. Skin Cancer: Recognition and Management, 2nd ed. Malden, MA: Blackwell Publishing; 2008:47–65.
  2. D’Souza J, Clark J. Management of the neck in metastatic cutaneous squamous cell carcinoma of the head and neck. Curr Opin Otolaryngol Head Neck Surg 2011; 19:99–105.
  3. Zbar RI, Canady JW. MOC-PSSM CME article: Nonmelanoma facial skin malignancy. Plast Reconstr Surg 2008; 121(suppl 1):1–9.
  4. Morselli P, Masciotra L, Pinto V, Zollino I, Brunelli G, Carinci F. Clinical parameters in T1N0M0 lower lip squamous cell carcinoma. J Craniofac Surg 2007; 18:1079–1082.
  5. American Joint Commission on Cancer. Cancer Staging Manual. 7th ed. http://www.cancerstaging.org. Accessed February 3, 2013.
  6. Lardaro T, Shea SM, Sharfman W, Liégeois N, Sober AJ. Improvements in the staging of cutaneous squamous-cell carcinoma in the 7th edition of the AJCC Cancer Staging Manual. Ann Surg Oncol 2010; 17:1979–1980.
  7. Cutaneous squamous cell carcinoma and other cutaneous carcinomas. In:Edge SB, Byrd DR, Compton CC, Fritz AG, Greene FL, Trotti A, editors. AJCC Cancer Staging Manual. 7th ed. New York, NY: Springer; 2010:301–314.
  8. Frierson HF, Cooper PH. Prognostic factors in squamous cell carcinoma of the lower lip. Hum Pathol 1986; 17:346–354.
  9. Civantos FJ, Moffat FL, goodwin WJ. Lymphatic mapping and sentinel lymphadenectomy for 106 head and neck lesions: contrasts between oral cavity and cutaneous malignancy. Laryngoscope 2006; 112(3 Pt 2 suppl 109):1–15.
  10. Rowe De, Carroll RJ, Day CL. Prognostic factors for local recurrence, metastasis, and survival rates in squamous cell carcinoma of the skin, ear, and lip. Implications for treatment modality selection. J Am Acad Dermatol 1992; 26:976–990.
  11. Veness MJ, Palme CE, Smith M, Cakir B, Morgan GJ, Kalnins I. Cutaneous head and neck squamous cell carcinoma metastatic to cervical lymph nodes (nonparotid): a better outcome with surgery and adjuvant radiotherapy. Laryngoscope 2003; 113:1827–1833.
References
  1. Schwartz RA. Squamous cell carcinoma. In:Schwartz RA, editor. Skin Cancer: Recognition and Management, 2nd ed. Malden, MA: Blackwell Publishing; 2008:47–65.
  2. D’Souza J, Clark J. Management of the neck in metastatic cutaneous squamous cell carcinoma of the head and neck. Curr Opin Otolaryngol Head Neck Surg 2011; 19:99–105.
  3. Zbar RI, Canady JW. MOC-PSSM CME article: Nonmelanoma facial skin malignancy. Plast Reconstr Surg 2008; 121(suppl 1):1–9.
  4. Morselli P, Masciotra L, Pinto V, Zollino I, Brunelli G, Carinci F. Clinical parameters in T1N0M0 lower lip squamous cell carcinoma. J Craniofac Surg 2007; 18:1079–1082.
  5. American Joint Commission on Cancer. Cancer Staging Manual. 7th ed. http://www.cancerstaging.org. Accessed February 3, 2013.
  6. Lardaro T, Shea SM, Sharfman W, Liégeois N, Sober AJ. Improvements in the staging of cutaneous squamous-cell carcinoma in the 7th edition of the AJCC Cancer Staging Manual. Ann Surg Oncol 2010; 17:1979–1980.
  7. Cutaneous squamous cell carcinoma and other cutaneous carcinomas. In:Edge SB, Byrd DR, Compton CC, Fritz AG, Greene FL, Trotti A, editors. AJCC Cancer Staging Manual. 7th ed. New York, NY: Springer; 2010:301–314.
  8. Frierson HF, Cooper PH. Prognostic factors in squamous cell carcinoma of the lower lip. Hum Pathol 1986; 17:346–354.
  9. Civantos FJ, Moffat FL, goodwin WJ. Lymphatic mapping and sentinel lymphadenectomy for 106 head and neck lesions: contrasts between oral cavity and cutaneous malignancy. Laryngoscope 2006; 112(3 Pt 2 suppl 109):1–15.
  10. Rowe De, Carroll RJ, Day CL. Prognostic factors for local recurrence, metastasis, and survival rates in squamous cell carcinoma of the skin, ear, and lip. Implications for treatment modality selection. J Am Acad Dermatol 1992; 26:976–990.
  11. Veness MJ, Palme CE, Smith M, Cakir B, Morgan GJ, Kalnins I. Cutaneous head and neck squamous cell carcinoma metastatic to cervical lymph nodes (nonparotid): a better outcome with surgery and adjuvant radiotherapy. Laryngoscope 2003; 113:1827–1833.
Issue
Cleveland Clinic Journal of Medicine - 80(4)
Issue
Cleveland Clinic Journal of Medicine - 80(4)
Page Number
222-224
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Cleveland Clinic Journal of Medicine
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Oncology
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A rapidly growing crusted nodule on the lip
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