Indian Journal of Dermatology
  Publication of IADVL, WB
  Official organ of AADV
Indexed with Science Citation Index (E) , Web of Science and PubMed
 
Users online: 2365  
Home About  Editorial Board  Current Issue Archives Online Early Coming Soon Guidelines Subscriptions  e-Alerts    Login  
    Small font sizeDefault font sizeIncrease font size Print this page Email this page


 
CASE REPORT
Year : 2010  |  Volume : 55  |  Issue : 3  |  Page : 284-289
Desmoplastic melanoma presenting as pyogenic granuloma: Report of a case with review of literature


Department of Plastic Surgery, New Medical Centre Specialty Hospital, Abu Dhabi, United Arab Emirates

Date of Web Publication25-Sep-2010

Correspondence Address:
B Venkata Ratnam
Head, Department of Aesthetic and Reconstructive Plastic Surgery, New Medical Centre Specialty Hospital, PO Box - 462 22, Abu Dhabi
United Arab Emirates
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0019-5154.70706

Rights and Permissions

   Abstract 

An elderly female patient was referred to the author for the treatment of a large recurrent pyogenic granuloma in the sole of right foot for a period of 2 years. She underwent excisional surgeries at an outside facility twice in the past. This time, she was treated with wide excision biopsy and the surgical defect was closed with a new technique, the "adjustable suture technique". Histopathology report confirmed "desmoplastic melanoma" with complete marginal clearance. The wound had healed uneventfully. There were no recurrences at 4-year follow-up.


Keywords: Desmoplastic melanoma, pyogenic granuloma, resemblance


How to cite this article:
Ratnam B V. Desmoplastic melanoma presenting as pyogenic granuloma: Report of a case with review of literature. Indian J Dermatol 2010;55:284-9

How to cite this URL:
Ratnam B V. Desmoplastic melanoma presenting as pyogenic granuloma: Report of a case with review of literature. Indian J Dermatol [serial online] 2010 [cited 2020 Feb 28];55:284-9. Available from: http://www.e-ijd.org/text.asp?2010/55/3/284/70706



   Introduction Top


Conditions without characteristic clinical features, especially if they are rare, can lead to incorrect diagnoses and management. The consequences could be fatal, but might be preventable with a high index of suspicion that follows familiarity with the condition. To the author's knowledge, desmoplastic melanoma, a rare and disastrous malignancy, presenting as pyogenic granuloma, a common and benign condition, has not been reported yet. This study reports one such case that had misled the treating doctors repeatedly.


   Case Report Top


This article reports the case of an elderly woman who presented with a painless growth that used to bleed on touch in the sole of her right foot for a period of two years. It was excised twice earlier elsewhere. The details of the earlier presentation, surgery, or histopathology were not available.

It resembled a large pyogenic granuloma at the junction of instep sole and weight-bearing heel [Figure 1]. There was no similar lesion elsewhere in the body, and there was no evidence of regional or systemic involvement. During a wide excision biopsy procedure, a soft, pigmented nodule of about 1 Χ 1 cm size was noted in the subcutaneous tissue [Figure 2], which was also included in the specimen. The resultant defect was directly closed in fourteen days' period using the "adjustable suture technique," a type of external tissue expansion, initiated by the author. [1]
Figure 1: Desmoplastic melanoma appearing as a large pyogenic granuloma

Click here to view
Figure 2: The pigmented soft tissue nodule in the subcutaneous tissue (arrow)

Click here to view


At four-year follow-up, the wound had healed well and the scar was stable. There was no evidence of local recurrence. Systemic survey and hematological and whole-body CT scanning at four-year follow-up were negative for metastases.

Histopathology

Separate Hematoxylin and Eosin stained sections from each lesion, the intervening tissue, and the surrounding tissues were examined microscopically.

The main lesion

It showed extensively ulcerated epidermis, covered by necrotic debris and fibrinoid exudates. It had infiltrative and expansile growth patterns in the dermis, extending into the subcutaneous tissue. It mainly consisted of two populations of cells given as follows: (i) The spindle cell population was predominant [Figure 3]. These cells were arranged in swirling fascicles, nests, and bundles exhibiting firoblast-like features. They had elongated, fusiform nuclei and showed mild to moderate degree of pleomorphism. Occasional foci of cells showed perivascular cuffing. In addition, focal storiform-areas, reminiscent of dermatofibrosarcoma protuberans (DFSP) and haemangiopericytoma-like (HPC-like) areas were also found [Figure 4]. The tumor cell mitoses were frequent, being about 30-35/10 high power fields [Figure 5]. (ii) The second cell type was the epithelioid cells [Figure 6] and [Figure 7]. They were present in nests and alveolar formations with vesiculated ovoid nuclei [Figure 7]. No cells contained melanin pigment in them. A moderate amount of lymphoplasmacytic infiltrate was present in the stroma [Figure 3]. The lesion was present at Clark's level V and Breslow's thickness of 8 mm, with microscopic evidence of all margins of surgical resection appearing free of tumor infiltration.
Figure 3: Intradermal location of tumor consisting mainly of spindle cells (vertical arrows) and lymphoplasmacytic infiltration (horizontal arrows) (H and E stain, ×50)

Click here to view
Figure 4: Tumor cells arranged in swirling fascicles reminiscent of DFSP (arrows) (H and E stain, ×100)

Click here to view
Figure 5: Spindle cells showing intense mitotic activity (arrows) (H and E stain, ×400)

Click here to view
Figure 6: Another area of same tumor showing epithelioid nature of the tumor cells (arrows) (H and E stain, ×100)

Click here to view
Figure 7: Epithelioid tumor cells with large vesicular nuclei and prominent nucleoli and eosinophilic cytoplasm (H and E stain, ×400)

Click here to view


The second lesion

It consisted of small-to moderate-sized cells with small, round nuclei, arranged in alveolar formations and nests [Figure 8]. No spindle cells were seen. A small proportion of these cells showed pale-brown, melanin pigment in their cytoplasm. A moderate amount of lymphoplasmacytic infiltrate was present in its stroma.
Figure 8: Satellite lesion consisting predominantly of epithelioid tumor cells on the right and fibrous intervening stroma on the left (H and E stain, ×50)

Click here to view


The fibro-fatty subcutaneous tissue between the two lesions

It was free of tumor cells [Figure 8].

Immunohistochemistry

The tumor cells in both the lesions showed diffuse positivity for S-100 [Figure 9] and vimentin [Figure 10], but negativity for cytokeratin [Figure 11]. The cells of the second lesion showed generalized positivity for HMB-45 [Figure 12], but this finding was scanty in the cells of the main lesion.
Figure 9: Immunohistochemical staining for S100 - diffuse positivity (Immunoperoxidase, ×400)

Click here to view
Figure 10: Immunohistochemical staining for Vimentin - strongly positive (Immunoperoxidase, ×100)

Click here to view
Figure 11: Immunohistochemical staining for Cytokeratin - negative (Immunoperoxidase, ×100)

Click here to view
Figure 12: Immunohistochemical staining for HMB 45 - weakly positive (Immunoperoxidase, ×400)

Click here to view


Systemic survey

Detailed hematological and whole-body CT scanning both initially and at four-year follow-up were negative for distant metastases.

Tissue diagnosis

Spindle cell variant of the "combined form" of cutaneous desmoplastic type of amelanocytic melanoma, in vertical growth phase, with marginal clearance and probable satellitism.

Final diagnosis and staging

Considering the history of repeated attempts at its excision, microscopic finding of scar tissue around the lesions, and the histopathological as well as immunohistochemical features mentioned earlier, the final diagnosis was made as recurrent cutaneous desmoplastic melanoma with macroscopic satellitism, which, as per the new AJCC classification, [2] belongs to: Clinical stage II C (T4b N0 M0) and pathological stage III b (T4 N2C M0).


   Literature Review Top


Conley et al. described "desmoplastic melanoma" in 1971. [3] Subsequently, a vast amount of literature was published about this rare entity. The salient features, in general, of its presentation such as site and clinical appearance, biological behaviour, histopathology and treatment recommendations were found to be common to most, if not all, of the publications, and they are mentioned below.

Epidemiology

Incidence: 1-2% of all melanomas, De Vita, 2005. [4]

Race: All races, but common in Caucasians.

Sex: Male : Female ratio = 1.75-2 : 1.

Age: Later age group, commonest in the seventh decade of life, Jain S et al., 1989. [5]

Site

It can occur in skin and mucosa of any region of the body. More commonly reported areas of occurrence are as follows:

Males: Sun-exposed areas on the head, neck, and upper part of the trunk.

Females: The extremities.

Size

Tends to be bulky, many lesions are not recognized until they have reached a substantial thickness.

Category

Neurectodermal tumor, Carlson JA, 1975 [6] /Neural crest tumor, Huttenbach, 2002. [7] Origin: Both from intraepidermal melanocytes as well as de novo, Carlson JA, 1995. [6] Type: Fibrosing variant of spindle cell melanoma, Busam KJ, 2005. [8]

Biological behaviour

  1. Locally aggressive

    High incidence of local recurrences.

    Recurrences are attributed to inadequate excision of the primary lesion.

    History of repeated surgeries with erroneous/mistaken diagnoses.

    Possibility of aggressive local treatment producing cure. [9]
  2. Lymph node metastases: Rare.
  3. Distant metastases: Rare. When present, they are common in the lungs.
  4. Radiotherapy and Chemotherapy: No proved effectiveness.


Clinical features

  1. Usually nonpigmented lesions.
  2. Often mistaken clinically for a scar, a fibroma, a basal cell carcinoma, a fleshy or firm nodule reminiscent of a scar, a sarcoma, or a dermatofibroma.
  3. Arise de novo or in association with a pre-existing lesion such as lentigo maligna, in which case, a clue to the diagnosis will be available.
  4. When de novo, they can present in an unsuspecting manner such as indurated, nonulcerated, and slightly elevated plaque, as a papule, or as a small nodule etc.


Till date, to the author's knowledge, no report exists describing it presenting as a pyogenic granuloma.


   Histopathology Top


Microscopic features

Desmoplasia, Busam, 2005, [8] Markovic et al., 2007 [10] : Spindle cells (amelanotic, fusiform, melanocytes) dispersed in a prominent collagenous or fibrous tissue stroma. The pure forms contain desmoplasia in more than 90% of the lesion. The combined or mixed forms contain desmoplasia in less than 10% of the lesion, with or without heteromorphism (presence of disparate phenotypes in a single neoplasm). The phenotypic elements include: epithelioid cells, Murali et al., 2008, [11] macrophages, smooth muscle, fibroblast-like cells, multinucleated cells, heterotopic bone, lentigo maligna epidermal component, nerve filaments, perivascular lymphoproliferation and focal lymphocytic aggregates.

Other histological features

They include ulceration, neurotropism, neuroma-like features, cytological atypia, atypical nuclei, high mitotic rate, higher mitotic index, stromal myxoid change, sarcoma-like features, individual necrotic cells, areas of myxoid or storiform appearance, infiltration of the adventitia of the blood vessels, perineurium, endoneurium or local nerves, vertical growth phase while arising in a pre-existing lesion such as a lentigo maligna, common depth of Breslow's measurement of more than 4 mm, and satellite lesions that are usually microscopic.

Immunohistochemistry

Diffuse positivity for S-100 and Vimentin, weak positivity or negativity for HMB 45, and negativity for Cytokeratin.

Diagnosis

Clinical presentation of "desmoplastic melanoma" is a diagnostic trap for the unwary, Mc Carthy et al., 2004. [12] The clinical and histological features of this lesion may give rise to perplexing diagnostic and therapeutic dilemmas. A high index of suspicion is warranted for its early and proper diagnosis.

Prognosis

Conventionally, the prognosis is considered poor, but it is a curable disease with aggressive local treatment alone, Arora et al., 2005. [13]


   Treatment Top


Wide excision

It alone may be sufficient. To be effective, all the excised specimens must be biopsied, and marginal clearance must be ensured in all the excised specimens. In the absence of marginal clearance, excisional surgery must be repeated until marginal clearance is ensured. Inadequate local treatment leads to local recurrence. Repeated local recurrences can lead to increased incidence of distant metastases. Death is usually due to distant metastases.

Sentinel lymph node biopsy

It is not usually helpful.

Follow-up

A careful, long-term follow-up is mandatory.


   Discussion Top


In the reported case, the nature of initial presentation to dermatologists and operating surgeons of the outside facility was unknown. It had recurred twice after the earlier surgeries. The simple precaution of ensuring the histological "marginal clearance" after the current surgical excision seemed to have made the difference. The local and systemic surveys that were negative at four-year follow-up suggest that, as per Lens et al., the condition can be considered as "cured". [14]

The "adjustable sutures" [1] are mattress sutures applied between the wound edges. Soft materials such as sterile dental rolls are used as bolsters. They are inserted between suture material and skin on either side of the wound, and are retained in place with a slipknot. Loosening of the slipknot, changing of the sterile dental rolls, gentle tightening of the sutures within the pain-tolerance-limit of the patient, and reapplication of the slipknot daily or on alternate days, gradually pulls the wounds' edges. With time, the wound edges meet each other, permitting direct closure of the wounds and avoiding the need for plastic surgical procedures such as skin grafting, flaps and microsurgery.


   Conclusion Top


In most cases, a DM is diagnosed only in established long-standing and thick melanomas. Therefore, dermatologists and dermatopathologists should be more aware of this clinicopathologic variant of cutaneous malignant melanoma, de Almeida et al., 2008. [15] Accordingly, this case was reported to increase familiarity of treating physicians with this misleading and disastrous malignancy presenting in an innocent manner; and to introduce a simple technique to close the "difficult-to-close" excisional defects that can be used by surgeons of all specialties and capacities.


   Acknowledgements Top


The author gratefully acknowledges the patient and her family members for their kind cooperation during the treatment, Padma Shri Dr. BR Shetty and Dr. CR Shetty, our Managing Director and Group Medical Director, respectively, for their encouragement and support, Dr. Sukrith Shetty, Head of Surgical Oncology, NMCSH, Dubai, for his suggestions in formulating treatment protocol, Dr. M. Chitradevi and Dr. Shakeel Akhtar, Heads of Pathology at NMC Hospitals, Abu Dhabi and Dubai respectively, for their help in preparing the photomicrographs and their related text, and Dr. B. Thejaswi Venkata Ratnam, Internee, Kasturba Hospital, Manipal, Manipal University, Karnataka, India. for her help in literature review and preparation of manuscript.

 
   References Top

1.B. Venkata Ratnam. Adjustable suture technique based on viscoelastic properties of skin for direct closure of a defect after abdominoplasty flap necrosis. Aesthetic Plast Surg 2006;30:497- 9.  Back to cited text no. 1      
2.Balch CM, Buzaid AC, Soong SJ, Atkins MB, Cascinelli N, Coit DG, et al. Final version of the American Joint Committee on Cancer staging system for cutaneous melanoma. J Clin Oncol 2001;19:3635-48.  Back to cited text no. 2      
3.Conley J, Lattes R, Orr W. Desmoplastic Malignant Melanoma (a rare variant of spindle cell melanoma). Cancer 1971;28:914-36.  Back to cited text no. 3      
4.Vincent T. De Vita Jr, Hellman S, Rosenberg, SA, editors. Cancer, Principles and Practice of Oncology. 7 th ed. Lippincott Williams and Wilkins; 2005.  Back to cited text no. 4      
5.Jain S, Allen PW. Desmoplastic malignant melanoma and its variants. A study of 45 cases. Am J Surg Pathol 1989;13:358-73.  Back to cited text no. 5      
6.Carlson LA, Dickersin GR, Sober AJ, Barnhill RL. Desmoplastic neurotropic melanoma. A clinicopathologic analysis of 28 cases. Cancer 1995;75:478-94.  Back to cited text no. 6      
7.Huttenbach Y, Prieto VG, Reed JA. Desmoplastic and spindle cell melanomas express protein markers of the neural crest but not of later committed stages of Schwann cell differentiation. J Cut Pathol 2002;29:562-8.  Back to cited text no. 7      
8.Busam KJ. Cutaneous Desmoplastic Melanoma. Adv Anat Pathol 2005;12:92-102.  Back to cited text no. 8      
9.Phillip R Casson and Perry Robins: Malignant tumors of the skin. In: G McCarthy JG, editor. Plastic Surgery. Vol. 5. WB Saunders Company; 1990. p. 3614-62.  Back to cited text no. 9      
10.Markovic SN, Erickson LA, Rao RD, Weenig RH, Pockaj BA, Bardia A, et al. Malignant melanoma in the 21st century, part 1: Epidemiology, risk factors, screening, prevention, and diagnosis. Mayo Clin Proc 2007;82:364-80.  Back to cited text no. 10      
11.Murali R, Loughman NT, McKenzie PR. Watson GF, Thompson JF, Scolyer RA. Cytologic features of metastatic and recurrent melanoma in patients with primary cutaneous desmoplastic melanoma. Am J Clin Pathol 2008;130:715-23.  Back to cited text no. 11      
12.McCarthy SW, Scolyer RA, Palmer AA. Desmoplastic melanoma: A diagnostic trap for the unwary. Pathology 2004;36:445-51.  Back to cited text no. 12      
13.Arora A, Lowe L, Su L, Rees R. Bradford C, Cimmino VC, et al.Wide excision without radiation for desmoplastic melanoma. Caner 2005;104:1462-7.  Back to cited text no. 13      
14.Lens MB, Newton-Bishop JA, Boon AP. Desmoplastic malignant melanoma: A systematic review. Br J Dermatol 2005;152:673-8.   Back to cited text no. 14      
15.de Almeida LS, Requena L, Rόtten A, Kutzner H, Garbe C, Pestana D, Gomes MM. Desmoplastic malignant melanoma: A clinicopathologic analysis of 113 cases. Am J Dermatopathol 2008;30:207-15.  Back to cited text no. 15      


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10], [Figure 11], [Figure 12]



 

Top
Print this article  Email this article
 
  Search
 
   Next article
   Previous article 
   Table of Contents
  
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Article in PDF (3,643 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    Abstract
    Introduction
    Case Report
    Literature Review
    Histopathology
    Treatment
    Discussion
    Conclusion
    Acknowledgements
    References
    Article Figures

 Article Access Statistics
    Viewed4597    
    Printed94    
    Emailed0    
    PDF Downloaded66    
    Comments [Add]    

Recommend this journal