<p>A 75-year-old Japanese man had a history of Stage IVb squamous cell lung cancer (cT3N1M1c) with metastases to the right ribs and left adrenal gland. He had previously tested negative for key nonsmall cell lung cancer driver mutations, including epidermal growth factor receptor, anaplastic lymphoma kinase, C-ros oncogene 1, v-raf murine sarcoma viral oncogene homolog B1 and programmed cell death protein 1. He presented with a painful nodule on the distal phalanx of his left fifth finger. The nodule had gradually increased to 3 cm in diameter and had a red, vascular surface (Figure 1). Initially, the nodule was diagnosed as paronychia and treated with antibiotics, but the condition did not improve. Radiography revealed complete destruction of the distal phalanx (Figure 2), and positron emission tomography-computed tomography showed abnormal uptake in the lesion. A biopsy was performed from the lesion on the left fifth finger (Figure 3a,b).</p><p>The patient was treated with a combination of pembrolizumab and cytotoxic anticancer agents, including paclitaxel and carboplatin. After starting treatment, the acrometastasis shrank dramatically and almost disappeared within 3 months (Figure 4) and dropped off spontaneously 5 months after treatment initiation. However, the patient's condition deteriorated due to the progression of the primary lung cancer, leading to a transition to palliative care. He passed away 2 weeks later.</p><p>Acrometastases refer to secondary lesions located distal to the elbow and knee, accounting for 0.1% of all bone metastases.<span><sup>1</sup></span> They are often misdiagnosed due to their rarity, with 56.8% of hand or wrist lesions initially mistaken for infections such as abscess, felon, osteomyelitis, paronychia or tuberculosis.<span><sup>2</sup></span> Symptoms typically include redness, swelling, pain and limited movement. Because patients with cancer typically have the primary tumour identified first, acrometastases should be considered in the differential diagnosis of distal lesions in patients with cancer.<span><sup>3, 4</sup></span> Our patient had a bone metastasis of lung cancer in the distal phalynx, which is the most common site of phalyngeal metastases.<span><sup>5</sup></span> Acrometastases may occur on either the right or left hand, with bilateral metastases being relatively rare.<span><sup>2</sup></span> The primary site in our patient was situated in the middle lobe of the left lung, disseminating to the right ribs and left adrenal gland. Notably, phalangeal metastases exhibit a nonlateralized distribution pattern with no discernible association with the laterality of the primary neoplasm, regardless of whether it is in the lung, breast or kidney.</p><p>The pathophysiology of acrometastasis is not fully understood but is believed to involve the hematogenous spread of tumour emboli. Mulvey et al.<span><sup>6</sup></span> speculated that venous erosion by a pulmonary neoplasm allows tumour emboli to dissem
{"title":"Painful nodule on the left fifth finger","authors":"Chihiro Hishinuma, Yuko Watanabe, Hideyuki Ishikawa, Atsuhito Nakazawa, Yukie Yamaguchi","doi":"10.1002/jvc2.583","DOIUrl":"https://doi.org/10.1002/jvc2.583","url":null,"abstract":"<p>A 75-year-old Japanese man had a history of Stage IVb squamous cell lung cancer (cT3N1M1c) with metastases to the right ribs and left adrenal gland. He had previously tested negative for key nonsmall cell lung cancer driver mutations, including epidermal growth factor receptor, anaplastic lymphoma kinase, C-ros oncogene 1, v-raf murine sarcoma viral oncogene homolog B1 and programmed cell death protein 1. He presented with a painful nodule on the distal phalanx of his left fifth finger. The nodule had gradually increased to 3 cm in diameter and had a red, vascular surface (Figure 1). Initially, the nodule was diagnosed as paronychia and treated with antibiotics, but the condition did not improve. Radiography revealed complete destruction of the distal phalanx (Figure 2), and positron emission tomography-computed tomography showed abnormal uptake in the lesion. A biopsy was performed from the lesion on the left fifth finger (Figure 3a,b).</p><p>The patient was treated with a combination of pembrolizumab and cytotoxic anticancer agents, including paclitaxel and carboplatin. After starting treatment, the acrometastasis shrank dramatically and almost disappeared within 3 months (Figure 4) and dropped off spontaneously 5 months after treatment initiation. However, the patient's condition deteriorated due to the progression of the primary lung cancer, leading to a transition to palliative care. He passed away 2 weeks later.</p><p>Acrometastases refer to secondary lesions located distal to the elbow and knee, accounting for 0.1% of all bone metastases.<span><sup>1</sup></span> They are often misdiagnosed due to their rarity, with 56.8% of hand or wrist lesions initially mistaken for infections such as abscess, felon, osteomyelitis, paronychia or tuberculosis.<span><sup>2</sup></span> Symptoms typically include redness, swelling, pain and limited movement. Because patients with cancer typically have the primary tumour identified first, acrometastases should be considered in the differential diagnosis of distal lesions in patients with cancer.<span><sup>3, 4</sup></span> Our patient had a bone metastasis of lung cancer in the distal phalynx, which is the most common site of phalyngeal metastases.<span><sup>5</sup></span> Acrometastases may occur on either the right or left hand, with bilateral metastases being relatively rare.<span><sup>2</sup></span> The primary site in our patient was situated in the middle lobe of the left lung, disseminating to the right ribs and left adrenal gland. Notably, phalangeal metastases exhibit a nonlateralized distribution pattern with no discernible association with the laterality of the primary neoplasm, regardless of whether it is in the lung, breast or kidney.</p><p>The pathophysiology of acrometastasis is not fully understood but is believed to involve the hematogenous spread of tumour emboli. Mulvey et al.<span><sup>6</sup></span> speculated that venous erosion by a pulmonary neoplasm allows tumour emboli to dissem","PeriodicalId":94325,"journal":{"name":"JEADV clinical practice","volume":"4 1","pages":"364-367"},"PeriodicalIF":0.0,"publicationDate":"2024-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jvc2.583","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143530117","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Stephanie Bowe conceived and designed the analysis, collected the data, contributed data or analysis tools, performed the analysis, wrote the paper. Claire Quigley collected data at pigmented lesion clinics via paper forms. Liana Victory collected data at pigmented lesion clinics via paper forms. Eoin Storan supervised the project and edited the final paper.
The authors declare no conflict of interest.
All subjects gave their informed consent for inclusion before they participated in the study. The study was conducted in accordance with the Declaration of Helsinki, and the protocol was approved by the MMUH and Mater Private Hospital Dublin Institutional Review Board at a meeting in October 2022, with the project reference number: 1/378/2322.
{"title":"A reply to “Letter to the editor in response to the article ‘To assess the attitudes of Irish patients attending a pigmented lesion clinic and healthcare staff employed in an academic hospital to biobanking, a quantitative study’”","authors":"Stephanie Bowe, Claire Quigley, Liana Victory, Eoin Storan","doi":"10.1002/jvc2.558","DOIUrl":"https://doi.org/10.1002/jvc2.558","url":null,"abstract":"<p>Stephanie Bowe conceived and designed the analysis, collected the data, contributed data or analysis tools, performed the analysis, wrote the paper. Claire Quigley collected data at pigmented lesion clinics via paper forms. Liana Victory collected data at pigmented lesion clinics via paper forms. Eoin Storan supervised the project and edited the final paper.</p><p>The authors declare no conflict of interest.</p><p>All subjects gave their informed consent for inclusion before they participated in the study. The study was conducted in accordance with the Declaration of Helsinki, and the protocol was approved by the MMUH and Mater Private Hospital Dublin Institutional Review Board at a meeting in October 2022, with the project reference number: 1/378/2322.</p>","PeriodicalId":94325,"journal":{"name":"JEADV clinical practice","volume":"3 5","pages":"1716-1717"},"PeriodicalIF":0.0,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jvc2.558","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142762667","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. Subhadarshani, L. E. Flowers, C. Logan, K. E. Spicknall, C. Shaughnessy
Iododerma is a rare halogenoderma resulting from exposure to iodinated compounds. We present a case involving a 51-year-old Caucasian female with advanced renal disease who developed a hemorrhagic and papulonodular eruption following oral contrast exposure. Cryptococcoid bodies were noted on histopathological evaluation and raised suspicion for the diagnosis of iododerma, which was ultimately confirmed through serum and urine iodine studies. This case highlights a severe presentation of iododerma with important dermatopathology findings.
{"title":"Iododerma with cryptococcus-like changes","authors":"S. Subhadarshani, L. E. Flowers, C. Logan, K. E. Spicknall, C. Shaughnessy","doi":"10.1002/jvc2.588","DOIUrl":"https://doi.org/10.1002/jvc2.588","url":null,"abstract":"<p>Iododerma is a rare halogenoderma resulting from exposure to iodinated compounds. We present a case involving a 51-year-old Caucasian female with advanced renal disease who developed a hemorrhagic and papulonodular eruption following oral contrast exposure. Cryptococcoid bodies were noted on histopathological evaluation and raised suspicion for the diagnosis of iododerma, which was ultimately confirmed through serum and urine iodine studies. This case highlights a severe presentation of iododerma with important dermatopathology findings.</p>","PeriodicalId":94325,"journal":{"name":"JEADV clinical practice","volume":"4 1","pages":"269-272"},"PeriodicalIF":0.0,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jvc2.588","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143530636","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}