brand logo

Am Fam Physician. 2022;105(4):425-426

Author disclosure: No relevant financial relationships.

A 65-year-old man presented with an erythematous mass on his thumb that had been slowly enlarging over 10 years. The mass was nontender but bled occasionally and increasingly interfered with daily activities. The patient did not have fever, chills, or night sweats.

Physical examination revealed a large, semifirm, mobile mass on the volar aspect of the right thumb (Figure 1). The lesion was not ulcerated. There was no lymphadenopathy. The affected hand had normal strength, sensation, and range of motion.

Plain radiography showed a soft tissue mass without evidence of a foreign body. Magnetic resonance imaging showed an exophytic superficial soft tissue mass measuring 3.7 × 3.0 × 3.7 cm without evidence of internal fat, cystic nature, foreign body, or involvement of the underlying tendon. The mass was excised, and pathologic examination showed diffuse subcutaneous fibrosis and granulomatous inflammation comprised of epithelioid histiocytes.

Question

Based on the patient’s history, physical examination findings, and additional testing, which one of the following is the most likely diagnosis?

  • A. Actinomycetoma.

  • B. Dermatofibroma.

  • C. Foreign body granuloma.

  • D. Giant cell tumor of the tendon sheath.

  • E. Invasive squamous cell carcinoma.

Discussion

The answer is A: actinomycetoma. Actinomycetoma is a painless, chronic, inflammatory, granulomatous, suppurative cutaneous lesion caused by Actinomadura, Nocardia, or Streptomyces bacteria, which are commonly found in soil. Mycetomas can be differentiated into actinomycetomas (caused by non–acid-fast bacterial infections) and eumycetoma (caused by fungal infections).1

Mycetomas present clinically as nodules, abscesses, fistulae, and swelling. The lesions usually involve the lower extremities but can also occur on the hands. Tendons and nerves are spared until late in the disease process. The disease is typically spread via lymphatic and hematologic systems. Mycetomas can cause distortions, disfigurement, and disability.2 If left untreated, they can cause superinfections, osteomyelitis, and ankylosis.1,2 Rarely, mycetomas are aggressive and can progress systemically, involving pelvic organs, the spinal cord, and lungs, with a high mortality rate.2

Gram stain shows thin filaments (0.5 to 1 μm) with actinomycetomas,3 but thicker fungal hyphae are seen with eumycetomas. Classic histologic findings are suppurative granulomas with neutrophilic infiltrates surrounded by palisaded histiocytes.1 Methenamine silver stain is used to highlight filamentous bacteria.

Although evidence varies, common treatments for actinomycetomas include dapsone, streptomycin, and trimethoprim/sulfamethoxazole. The treatment duration and dosage are dependent on disease severity and tissue involvement.1,3 Surgical debulking may be an option for larger, more burdensome masses but has an increased risk of recurrence.1

Dermatofibromas are benign fibrous histiocytomas of the skin, usually related to trauma in the affected area. Lesions are typically firm and less than 1 cm in diameter. Histology shows proliferation of spindle-shaped fibrous cells and histiocytoid cells in a storiform pattern.4

Foreign body granulomas are caused by penetrating objects, typically made of glass, metal, or wood. Radiographic visualization depends on the material’s radiodensity. Magnetic resonance imaging is the best modality for identification of nonmetallic sources. Histology shows granulation tissue with fibroblasts and inflammatory infiltrates of lymphocytes, plasma cells, histiocytes, and giant cells.5

Giant cell tumor of the tendon sheath is the second most common benign neoplasm of the hand. It is a painless lesion of the soft tissues. Histology shows these lesions are composed of multinucleated giant cells, histiocytes, fibrotic material, and hemosiderin deposits.6

Invasive squamous cell carcinomas appear ulcerated and can be patchy, papulonodular, papillomatous, or exophytic lesions.7 They can also resemble their precursor, actinic keratosis lesions, but with evidence of infiltration of cells into the dermis. Histologically, they have atypical nuclei, pleomorphism, keratinization, or sometimes a pearl-like dermal nest. Patients may also present with weight loss, night sweats, and pain.8

ConditionCharacteristics
ActinomycetomaPainless, chronic, inflammatory, granulomatous, suppurative cutaneous lesion caused by Actinomadura, Nocardia, or Streptomyces bacteria; histology shows granulomas with neutrophilic infiltrate surrounded by palisaded histiocytes; Gram stain commonly shows thin filaments
DermatofibromaBenign fibrous histiocytomas of the skin; histology shows proliferation of spindle-shaped fibrous cells and histiocytoid cells in a storiform pattern
Foreign body granulomaGranuloma formation caused by a penetrating object, such as glass, metal, or wood; object often visible on plain radiography or magnetic resonance imaging; histology shows granulation tissue with fibroblasts and inflammatory infiltrates
Giant cell tumor of the tendon sheathPainless lesion of the soft tissues; histology shows these lesions are composed of multinucleated giant cells, histiocytes, fibrotic material, and hemosiderin deposits
Invasive squamous cell carcinomaUlcerated; can be patchy, papulonodular, papillomatous, or exophytic; histology shows atypical nuclei, pleomorphism, keratinization, or sometimes a pearl-like dermal nest; may be associated with weight loss, night sweats, and pain

The editors of AFP welcome submissions for Photo Quiz. Guidelines for preparing and submitting a Photo Quiz manuscript can be found in the Authors' Guide at https://www.aafp.org/afp/photoquizinfo. To be considered for publication, submissions must meet these guidelines. Email submissions to afpphoto@aafp.org.

This series is coordinated by John E. Delzell Jr., MD, MSPH, associate medical editor.

A collection of Photo Quiz published in AFP is available at https://www.aafp.org/afp/photoquiz

Continue Reading


More in AFP

More in PubMed

Copyright © 2022 by the American Academy of Family Physicians.

This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP.  See permissions for copyright questions and/or permission requests.