<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0" xmlns:media="http://search.yahoo.com/mrss/"><channel><title><![CDATA[Saleem Islam, MD, MPH]]></title><description><![CDATA[Thoughts, stories and ideas.]]></description><link>https://saleem.focalize.md/</link><image><url>https://saleem.focalize.md/favicon.png</url><title>Saleem Islam, MD, MPH</title><link>https://saleem.focalize.md/</link></image><generator>Ghost 4.19</generator><lastBuildDate>Thu, 09 Apr 2026 04:23:19 GMT</lastBuildDate><atom:link href="https://saleem.focalize.md/rss/" rel="self" type="application/rss+xml"/><ttl>60</ttl><item><title><![CDATA[Malignant melanoma in children.]]></title><description><![CDATA[<p>Six patients with prepubertal malignant melanoma are presented. Three were metastatic. One was congenital in a giant pigmented nevus. A second was found at 6 mo of age to have metastatic lesions. All were treated aggressively and had a favorable outcome. Aggressive treatment, once malignant melanoma is diagnosed, is recommended.</p>]]></description><link>https://saleem.focalize.md/malignant-melanoma-in-children-2/</link><guid isPermaLink="false">6175d749b52f7cb358269c31</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:37 GMT</pubDate><content:encoded><![CDATA[<p>Six patients with prepubertal malignant melanoma are presented. Three were metastatic. One was congenital in a giant pigmented nevus. A second was found at 6 mo of age to have metastatic lesions. All were treated aggressively and had a favorable outcome. Aggressive treatment, once malignant melanoma is diagnosed, is recommended. Prognosis does not differ markedly from similar lesions in adults.</p>]]></content:encoded></item><item><title><![CDATA[Sentinel lymph node biopsy for melanoma in young children.]]></title><description><![CDATA[<p>Lymphoscintigraphy and sentinel lymph node biopsy techniques can be applied successfully to young children with melanoma to detect nodal disease. The authors describe their methods of lymphoscintigraphy and sentinel node biopsy and its application in 2 young children with malignant melanoma of the head and neck.</p>]]></description><link>https://saleem.focalize.md/sentinel-lymph-node-biopsy-for-melanoma-in-young-children-2/</link><guid isPermaLink="false">6175d748b52f7cb358269c2d</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:36 GMT</pubDate><content:encoded><![CDATA[<p>Lymphoscintigraphy and sentinel lymph node biopsy techniques can be applied successfully to young children with melanoma to detect nodal disease. The authors describe their methods of lymphoscintigraphy and sentinel node biopsy and its application in 2 young children with malignant melanoma of the head and neck.</p>]]></content:encoded></item><item><title><![CDATA[Lymphatic mapping with sentinel node biopsy in pediatric patients.]]></title><description><![CDATA[<p>BACKGROUND/PURPOSE Lymphatic mapping with sentinel node biopsy is used widely in adult melanoma and breast cancer to determine nodal status without the morbidity associated with elective lymph node dissection. This technique can be used in children to determine lymph node status with limited dissection and accurate interpretation. The authors</p>]]></description><link>https://saleem.focalize.md/lymphatic-mapping-with-sentinel-node-biopsy-in-pediatric-patients-2/</link><guid isPermaLink="false">6175d748b52f7cb358269c29</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:36 GMT</pubDate><content:encoded><![CDATA[<p>BACKGROUND/PURPOSE Lymphatic mapping with sentinel node biopsy is used widely in adult melanoma and breast cancer to determine nodal status without the morbidity associated with elective lymph node dissection. This technique can be used in children to determine lymph node status with limited dissection and accurate interpretation. The authors report their initial experience. METHODS The charts of patients who underwent lymphatic mapping with sentinel node biopsy were reviewed retrospectively. Lymphoscintigraphy was performed in patients with truncal lesions 24 hours before surgery to determine the draining nodal basin (for surgical mapping). The tumors were injected 1 hour preoperatively with technetium sulfur colloid and in the operating room with Lymphazurin blue. The draining basin was examined using a radioisotope detector. The blue nodes with high counts were localized and removed. If nodal metastases were identified, lymph node dissection was recommended. Four patients were injected only with Lymphazurin blue. RESULTS Thirteen children (7 girls, 6 boys; mean age, 7 years) underwent lymphatic mapping with sentinel node biopsy. The tumor types were as follows: 8 malignant melanoma (6 extremity, 2 truncal), 1 malignant peripheral nerve sheath tumor, 1 alveolar soft part sarcoma, and 3 rhabdomyosarcoma. A mean of 2.4 nodes (range, 1 to 6) were removed from each patient. Six patients had a positive sentinel node. Formal lymph node dissection was performed on 4 of the 6 patients, 1 of whom had further nodal disease with 2 of 13 nodes containing micrometastases. One of the 6 patients refused lymph node dissection and adjuvant therapy; the final patient had rhabdomyosarcoma, a malignancy for which lymph node dissection is not indicated. Pulmonary metastasis developed 26 months after diagnoses in the patient with alveolar soft part sarcoma and a negative sentinel node. This patient was injected only with Lymphazurin blue at the time of sentinel node biopsy and refused adjuvant therapy. There have been no other recurrences. There were no complications related to lymphatic mapping or sentinel node biopsy. CONCLUSIONS Lymphatic mapping with sentinel node biopsy, using both technetium-labeled sulfur colloid and Lymphazurin blue, can be performed safely in pediatric skin and soft tissue malignancies. Further study with long-term follow-up will determine the utility and accuracy of this technique in pediatric malignancies.</p>]]></content:encoded></item><item><title><![CDATA[Assessment of value of the sentinel lymph node biopsy in melanoma in children and adolescents and applicability of subcutaneous infusion anesthesia.]]></title><description><![CDATA[<p>BACKGROUND/PURPOSE The management of pediatric melanoma is controversial but equates that of adults. Lymphatic mapping with sentinel lymph node (SLN) biopsy is proposed as standard of care for patients with primary melanoma. The operation can be done with general or local anesthesia in adults. The goal of this study</p>]]></description><link>https://saleem.focalize.md/assessment-of-value-of-the-sentinel-lymph-node-biopsy-in-melanoma-in-children-and-adolescents-and-applicability-of-subcutaneous-infusion-anesthesia-2/</link><guid isPermaLink="false">6175d748b52f7cb358269c25</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:36 GMT</pubDate><content:encoded><![CDATA[<p>BACKGROUND/PURPOSE The management of pediatric melanoma is controversial but equates that of adults. Lymphatic mapping with sentinel lymph node (SLN) biopsy is proposed as standard of care for patients with primary melanoma. The operation can be done with general or local anesthesia in adults. The goal of this study was to determine the applicability of subcutaneous infusion anesthesia (SIA) for SLN biopsy in children and adolescents, as well as to assess complications of this procedure and to document outcome of patients with melanoma in this particular age group after SLN biopsy. METHODS Charts of patients with melanomas on the trunk and extremities who underwent lymphatic mapping and SLN biopsy in SIA between November 2000 and January 2006 revealed 13 patients with age 21 years or less. Tumescent solutions with lidocaine (0.2%) were used for SLN biopsy. Patient demographics, tumor thickness, Clark level, location of primary melanoma, ulceration, number of SLNs, number of positive nodes, and follow-up of patients were included. RESULTS In 13 patients (age range, 12-21), SLN biopsy was performed. Mean tumor thickness was 1.8 mm (range, 1.0-7.0), none of these melanomas showed ulceration. The operation was tolerated in SIA by all patients; none had any associated complications. Of 13 patients, 5 (38.5%) had positive sentinel nodes. Three patients underwent completion lymph node dissection, and no further positive nodes were found. After a mean follow-up of 29.2 months (range, 13-68), all patients were found disease-free. CONCLUSIONS Sentinel lymph node biopsy in SIA can safely be performed in children and adolescents with primary melanomas. Further studies are necessary to determine the prognostic information and therapeutic implications of SLN biopsy in this patient group.</p>]]></content:encoded></item><item><title><![CDATA[Malignant melanoma in children: its management and prognosis.]]></title><description><![CDATA[<p>Malignant melanoma is rare in children, representing 1% to 3% of all pediatric malignancies. Thirty-three children with malignant melanoma were treated at St Jude Children&apos;s Research Hospital from 1967 to 1988. Their ages ranged from 1 day to 20 years (median, 12 years); 23 were boys and 10</p>]]></description><link>https://saleem.focalize.md/malignant-melanoma-in-children-its-management-and-prognosis-2/</link><guid isPermaLink="false">6175d748b52f7cb358269c21</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:36 GMT</pubDate><content:encoded><![CDATA[<p>Malignant melanoma is rare in children, representing 1% to 3% of all pediatric malignancies. Thirty-three children with malignant melanoma were treated at St Jude Children&apos;s Research Hospital from 1967 to 1988. Their ages ranged from 1 day to 20 years (median, 12 years); 23 were boys and 10 were girls; and 5 of the 33 (15%) were black. Four of the 33 children had been treated for a previous malignancy. In 3, melanoma arose within a bathing trunk nevus. The extremity was the most common site (13), followed by the trunk (9), head and neck (7), and perineum (1). In 3 patients the primary site could not be determined. Upon initial presentation to St Jude Hospital, 17 patients had localized disease (stage I), 10 had regional node involvement (stage II), and the remaining 6 patients had disseminated disease (stage III). Using both Clark&apos;s level and Breslow&apos;s thickness as indicators, the incidence, initial stage, prognosis, and survival were compared. By Clark&apos;s level, 7 patients, (6 of whom were stage I) were level II or III, and 22 patients were level IV or V. Though 16 of 22 level IV and V patients were initially stage I, 10 patients eventually developed progressive disease. Similar observations were noted when using Breslow&apos;s thickness to evaluate the primary. In 5 of 27 evaluable patients, Breslow&apos;s depth of invasion was less than 1.5 mm. All 5 of these patients were diagnosed with stage I disease and have not shown progressive disease.</p>]]></content:encoded></item><item><title><![CDATA[Childhood melanoma.]]></title><description><![CDATA[<p>In melanoma patients, the prognostic value of tumor depth, Clark&apos;s level, the presence of ulceration, and regional involvement have not been clearly documented in the pediatric population. This report correlates these factors in a population-based study of patients under the age of 20 years. Of the initial 35</p>]]></description><link>https://saleem.focalize.md/childhood-melanoma/</link><guid isPermaLink="false">6175d748b52f7cb358269c1d</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:36 GMT</pubDate><content:encoded><![CDATA[<p>In melanoma patients, the prognostic value of tumor depth, Clark&apos;s level, the presence of ulceration, and regional involvement have not been clearly documented in the pediatric population. This report correlates these factors in a population-based study of patients under the age of 20 years. Of the initial 35 melanoma patients registered in southern Alberta with the Alberta Cancer Board, 14 were found on review to have a diagnosis other than melanoma. In the remaining 21 cases the diagnosis of melanoma was confirmed. There was a suggestion that patients with deeper lesions had a worse prognosis, but this was statistically confirmed only using Clark&apos;s levels. The children were then compared with all melanoma patients diagnosed in southern Alberta over the same time period. There was no difference in tumor depth, Clark&apos;s level, ulceration, regional involvement, or survival between these two groups. The natural history in children appears to be similar to that of the adult population, contrary to previous reports suggesting a markedly worse prognosis.</p>]]></content:encoded></item><item><title><![CDATA[Complications in the surgical treatment of pediatric melanoma.]]></title><description><![CDATA[<p>PURPOSE The purpose of this study was to characterize the complications associated with surgical treatment of pediatric melanoma. METHODS We retrospectively reviewed all pediatric patients who received surgical treatment for melanoma at our institution between 1992 and 2010. We compared complications between three groups: wide local excision only (WLE), WLE</p>]]></description><link>https://saleem.focalize.md/complications-in-the-surgical-treatment-of-pediatric-melanoma/</link><guid isPermaLink="false">6175d748b52f7cb358269c19</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:36 GMT</pubDate><content:encoded><![CDATA[<p>PURPOSE The purpose of this study was to characterize the complications associated with surgical treatment of pediatric melanoma. METHODS We retrospectively reviewed all pediatric patients who received surgical treatment for melanoma at our institution between 1992 and 2010. We compared complications between three groups: wide local excision only (WLE), WLE and sentinel lymph node biopsy (SLNB), and WLE and completion lymph node dissection (CLND). RESULTS One hundred twenty-five patients were identified: 37 patients received WLE only, 47 received WLE and SLNB, and 41 patients had WLE and CLND. Complication rates differed between the three groups: 19% in WLE, 11% in WLE+SLNB, and 39% in WLE+CLND (P=.006). The risk of complications was significantly lower among patients having WLE+SLNB versus WLE+CLND (OR 0.19, 95% CI 0.06-0.57, P=.0032). Lymphedema was a common complication with a higher incidence in the CLND group compared to the SLNB group (19.5% vs. 2.1%, P=.01). Complications were more frequent in inguinal compared to axillary dissections (52.0% vs. 17.1%, P=.006). CONCLUSIONS In the surgical treatment of pediatric melanoma, the addition of a completion lymph node dissection significantly increases complication risk. Thus, it is critical to determine which patients truly benefit from this procedure.</p>]]></content:encoded></item><item><title><![CDATA[Melanoma incidence rises for children and adolescents: an epidemiologic review of pediatric melanoma in the United States.]]></title><description><![CDATA[<p>BACKGROUND/PURPOSE This study was conducted to determine the influence of age on disease presentation and evaluate the change in pediatric melanoma incidence between 1998 and 2007. METHODS We performed a retrospective review of all children &#x2264;18 years with cutaneous melanoma who were included in the 2007 National Cancer</p>]]></description><link>https://saleem.focalize.md/melanoma-incidence-rises-for-children-and-adolescents-an-epidemiologic-review-of-pediatric-melanoma-in-the-united-states/</link><guid isPermaLink="false">6175d748b52f7cb358269c15</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:36 GMT</pubDate><content:encoded><![CDATA[<p>BACKGROUND/PURPOSE This study was conducted to determine the influence of age on disease presentation and evaluate the change in pediatric melanoma incidence between 1998 and 2007. METHODS We performed a retrospective review of all children &#x2264;18 years with cutaneous melanoma who were included in the 2007 National Cancer Institute Surveillance, Epidemiology, and End Results (SEER) database between 1988 and 2007. RESULTS We identified a total of 1447 patients with cutaneous melanoma. The overall average annual melanoma incidence was 5.4 per 1 million children and adolescents in the U.S., which increased throughout the study period. Most patients (89%) were at least 10 years of age (average age 15 years). Melanoma in situ (21%), thin (&lt;1 mm) lesions (37%), stage I disease (46%), and superficial spreading histology (25%) were common at presentation. Only 1% of patients presented with distant metastases. Preadolescents younger than age 10 were ethnically more diverse and more likely to present with non-truncal primaries and advanced disease (P&lt;.01) compared to adolescents. CONCLUSIONS The incidence of pediatric melanoma in the U.S. is increasing. There are significant differences between children and adolescents which suggest age-based inherent differences in the biology of the disease may exist.</p>]]></content:encoded></item><item><title><![CDATA[Pediatric melanoma: a single-institution experience of 150 patients.]]></title><description><![CDATA[<p>PURPOSE Differentiating pigmented skin lesions from malignant melanoma in the pediatric population has been a challenge. Despite guidelines describing clinical features and histopathologic criteria to distinguish these lesions, misdiagnoses still occur. We report our experience over 30 years in a pediatric population with malignant melanoma. METHODS We performed a retrospective</p>]]></description><link>https://saleem.focalize.md/pediatric-melanoma-a-single-institution-experience-of-150-patients/</link><guid isPermaLink="false">6175d747b52f7cb358269c11</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:35 GMT</pubDate><content:encoded><![CDATA[<p>PURPOSE Differentiating pigmented skin lesions from malignant melanoma in the pediatric population has been a challenge. Despite guidelines describing clinical features and histopathologic criteria to distinguish these lesions, misdiagnoses still occur. We report our experience over 30 years in a pediatric population with malignant melanoma. METHODS We performed a retrospective review of 150 pediatric patients treated for malignant melanoma between 1973 and 2007 at our institution. Outcomes measured included age, Breslow thickness, Clark level of invasion, tumor location, local and distant failure rates, and overall survival. RESULTS One hundred fifty pediatric patients were evaluated. The mean age was 15.1 years. The mean Breslow thickness was 2.05 mm and corresponding Clark level of invasion was 3.47. There were 43 known recurrences (29%); 29 distant, 14 nodal, and 7 local. Overall survival was 84% with a mean follow-up of 8.5 years. Sixteen patients (10.7%) were incorrectly diagnosed on initial pathologic examination. Overall survival in the misdiagnosed group was 66%. CONCLUSION Pigmented skin lesions in the pediatric population represent a diagnostic challenge to pathologists and clinicians. Improvements in diagnostic techniques with rigorous characterization, as well as increased physician awareness, should lead to a reduction in errors of diagnosis.</p>]]></content:encoded></item><item><title><![CDATA[Sentinel lymph node biopsy for melanoma and other melanocytic tumors in adolescents.]]></title><description><![CDATA[<p>BACKGROUND/PURPOSE Melanoma is rare, accounting for only 1% of all pediatric malignancies. The management of pediatric melanoma is controversial but largely parallels that of an adult occurrence. Sentinel lymph node biopsy (SLNBX) has become a standard of care for adults with melanoma, but the role of this procedure in</p>]]></description><link>https://saleem.focalize.md/sentinel-lymph-node-biopsy-for-melanoma-and-other-melanocytic-tumors-in-adolescents/</link><guid isPermaLink="false">6175d747b52f7cb358269c0d</guid><dc:creator><![CDATA[Saleem Islam]]></dc:creator><pubDate>Sun, 24 Oct 2021 21:59:35 GMT</pubDate><content:encoded><![CDATA[<p>BACKGROUND/PURPOSE Melanoma is rare, accounting for only 1% of all pediatric malignancies. The management of pediatric melanoma is controversial but largely parallels that of an adult occurrence. Sentinel lymph node biopsy (SLNBX) has become a standard of care for adults with melanoma, but the role of this procedure in the staging of pediatric patients remains to be established. The goal of this study was to determine outcomes and complications of children and adolescent patients undergoing SLNBX at the authors&apos; institution. METHODS A retrospective review of patients younger than 21 years (N = 20) undergoing SLNBX for melanoma or other melanocytic skin lesions at the University of Colorado Health Science Center between 1996 and 2003 was conducted. RESULTS Sentinel lymph node biopsy was successful in all 20 patients, and 8 patients (40%) were found to have metastases within the sentinel node. As in adults, the sentinel node status correlates with primary tumor depth. No complications occurred in patients undergoing SLNBX, but 4 clinically significant complications (57%) occurred in the 7 patients undergoing a completion lymph node dissection. At 33 months median follow-up, all patients were disease free. CONCLUSIONS Sentinel lymph node biopsy can be successfully and safely performed in pediatric patients for melanoma and atypical nevi. However, the prognostic information and therapeutic implications of SLNBX results for children and adolescents remain unclear. Completion lymph node dissection for microscopic disease is a morbid procedure with uncertain benefit to pediatric or adult patients with a positive SLNBX result. Long-term follow-up data are needed before SLNBX can become a standard of care in pediatric melanoma or as a diagnostic tool to distinguish the atypical Spitz nevus from melanoma.</p>]]></content:encoded></item></channel></rss>