Page 102 - GTM-3-1
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Global Translational Medicine                                    Anergy in Leishmania-associated malignancy



              Despite the inconclusive evidence, numerous studies
            have linked  Leishmania sp. to cancer.  Pathologically,
                                            6-8
            the manifestations of leishmaniasis resemble those of
            cancer, and their appearance may precede those of cancer.
            A number of studies have reported the association between
            Leishmania sp. and the development of malignant lesions
            such as basal cell carcinoma, squamous cell carcinoma
            (SCC), leukemia and lymphoma, and hemangiosarcoma.
                                                          6
            Cutaneous SCC is the most common skin cancer among
            blacks and the second most common among Whites,
            Asians, and Hispanics. The mortality rate due to cutaneous
            SCC ranges from 1.5% to 3.4%, with nodal metastases
            occurring in 1.9% to 5.2% of cases,  but early diagnosis can
                                       7
            improve the prognosis. The risk of developing cutaneous
            SCC, the number of lesions, and the aggressiveness of
            each lesion can be augmented by congenital, acquired, and   Figure 1. Multiple nodular lesions, each measuring 5 – 12 mm in size,
            iatrogenic  immunosuppression.  Chronic  inflammation   that were deeply infiltrated and fused to the skin with purulent exudate-
            and infectious agents are other risk factors for developing   oozing ulcers of irregular margins.
            cutaneous SCC. 7
                                                                 The Montenegro skin test showed non-reactive outcome
              Here, we  report the  case of a  patient with diffuse   after 72 h, indicating positive anergy. Hematoxylin and eosin
            cutaneous leishmaniasis who developed cutaneous SCC in   staining showed severe chronic histiocytic inflammation
            the active lesions of leishmaniasis.               with multiple amastigotes in the tissue specimens (Figure 2).
            2. Case presentation                               DNA  amplification  testing assays were not  performed.
                                                               A biopsy procured from an ulcerated lesion unveiled SCC
            In  the  present  case,  we  report  a 63-year-old farmer   with mild coexistence of Leishmania sp. bodies (Figure 3).
            from Comalcalco, Tabasco, Mexico, suffering from     An axial computed tomography scan was performed,
            diffuse cutaneous leishmaniasis, which was diagnosed   uncovering imaging manifestations suggestive of cervical
            10  years ago. The parasitic disease had been treated   lymph node metastasis (Figure  4), a diagnosis that was
            intermittently  with  20  mg/kg  intramuscular  meglumine   later confirmed by histopathological examination. The
            antimonate (Glucantime) for 20 days, but the patient had   patient was treated with 3 mg/kg/day amphotericin B for
            a record of poor compliance in adhering to the prescribed   10 days and prescribed radiotherapy. However, the tumor
            medications. No relevant comorbidity was reported in his   exhibited poor response to radiotherapy, and the patient
            medical history, and his HIV ELISA result was negative.
                                                               did  not return to  the  hospital  for  follow-up  medical
              After being untreated for 6 months, several new lesions   consultations and interventions.
            appeared on the right side of the patient’s face, besides those
            that first appeared 4  months before the new additions.   3. Discussion
            The dermatosis consisted of multiple nodular lesions   SCC is the second most common malignancy that originates
            measuring 5 – 12 mm with deep infiltrates and deep, non-  from the skin.  Despite its multifactorial etiology, chronic
                                                                          7
            tender plaques (Figure  1). There were also ulcers with   sun exposure, pre-existing lesions (actinic keratosis,
            irregular margins oozing serous exudate, which reportedly   unhealed wounds, or scar known as Marjolin ulcer), and
            appeared 1 month before seeking medical consultation at   chronic infections (mainly viral diseases) are some of the
            our clinic. Bleeding was observed in two of these lesions   prominent the risk factors of SCC.  The occurrence of
                                                                                             7
            but was generally left unattended. No actinic keratosis was   skin cancer in the previous leishmaniasis lesions is a rare
            detected, and cervical examination did not reveal signs of   but an already reported phenomenon in the literature.
                                                                                                             8
            lymphadenopathy.                                   Older men with a long history of ultraviolet exposure are
              Several non-ulcerated and non-infiltrated nodules on   particularly vulnerable to the development of skin cancer
            the trunk and extremities measuring approximately 0.5 cm   on the prior lesion sites of leishmaniasis. Most of these
            in diameter were observed. These lesions were painless   tumors arise from previous leishmaniasis scars, although
            and flesh-colored. Some nodules had hemorrhagic crusts   there are reports of an association between active infection
            on the surface, fine scaling, and hyper- and hypo-chromic   and skin cancer. 8-12  However, to the best of our knowledge
            macular scarring.                                  and experience, such an association is rare.


            Volume 3 Issue 1 (2024)                         2                        https://doi.org/10.36922/gtm.2281
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