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13-year-old tuberous sclerosis patient with renal cell carcinoma associated with multiple renal angiomyolipomas developing multifocal micronodular pneumocyte hyperplasia
© Behnes et al.; licensee BioMed Central Ltd. 2013
Received: 25 September 2012
Accepted: 30 January 2013
Published: 5 February 2013
The autosomal dominant tumor syndrome tuberous sclerosis complex is caused by the mutated TSC1 gene, hamartin, and the TSC2 gene, tuberin. Patients with this complex develop typical cutaneus symptoms such as peau chagrin or angiofibromas of the skin as well as other lesions such as astrocytomas in the brain and lymphangioleiomyomatosis in the lung. Only a few tuberous sclerosis patients have been described who showed a multifocal micronodular pneumocyte hyperplasia of the lung. Another benign tumor which often occurs together with tuberous sclerosis is the angiomyolipoma of the kidney. Furthermore, an increased incidence of renal cell carcinoma in connection with tuberous sclerosis has also been proven.
We report a 13-year-old white girl with epilepsy and hypopigmented skin lesions. Radiological studies demonstrated the typical cortical tubers leading to the diagnosis of tuberous sclerosis. In the following examinations a large number of angiomyolipomas were found in both kidneys. One lesion showed an increasing size and tumor like aspects in magnetic resonance imaging. The pathological examination of the following tumorectomy demonstrated an unclassified renal cell carcinoma. Four months postoperatively, a follow-up computer tomography revealed multiple bilateral pulmonary nodules. To exclude lung metastases of the renal cell carcinoma, multiple open-lung biopsies were performed.
Here we report a diagnostically challenging case of a 13-year-old patient with tuberous sclerosis and angiomyolipomas of the kidney who developed an unclassified renal cell carcinoma as well as multifocal micronodular pneumocyte hyperplasia.
The TSC1 gene, hamartin, and the TSC2 gene, tuberin, were identified in 1997 and 1993, respectively. These tumor suppressor genes are mutated in the autosomal dominant tumor syndrome tuberous sclerosis complex (TSC) [1–3]. TSC is characterized by the formation of hamartomatous lesions in multiple organ systems. Besides the typical skin manifestations, e.g. cutaneous angiofibroma, peau chagrin, or subungual fibromas, TSC patients develop numerous brain lesions such as cortical tubers and subependymal giant cell astrocytomas. In addition, patients show an increased incidence of benign tumors such as multiple renal angiomyolipomas (AMLs), lymphangioleiomyomatosis (LAM) of the lungs, cardiac rhabdomyomas, and adenomatous polyps of the duodenum and the small intestine. Another rare manifestation of TSC is the so-called multifocal micronodular pneumocyte hyperplasia (MMPH), first recognized in 1991 by HH Popper . TSC is also associated with an increased incidence of renal cell carcinomas (RCC) .
In this report, we present a case of a young patient with TSC and multiple AMLs who developed a RCC as well as MMPH. We discuss the histological, immunohistological and molecular features of these lesions with emphasis on the diagnostic requirements and differential diagnosis.
Pathological findings of the renal tumors
Macroscopically, the tumorectomy revealed a 5 cm yellowish red tumor with multiple 1 to 2 mm yellow nodules in the adjacent kidney tissue.
The 5 cm tumor of the kidney showed a solid and nested, sometimes papillary architecture, and was composed of clear cells with voluminous cytoplasm, discrete cell borders, and vesicular chromatin. In addition, psammomatous calcification and hyaline nodules could be detected (Figure 1C). Immunohistochemical examinations revealed a weak to strong staining for vimentin and CD10 in more than 50% of neoplastic cells. All tumor cells showed a strong staining for P504s (Figure 1D). Pan-CK was only weakly expressed in scattered tumor cells. CK7 or HMB-45 could not be shown in the carcinoma cells. Based on the morphological and immunohistochemical findings, it was hypothesized that the tumor might be a RCC of XP 11.2 translocation type. This hypothesis was confirmed by three independent consultant pathologists (Leuschner I, Department of Pathology, University of Kiel, Germany; Moch H, Department of Surgical Pathology, University of Zürich, Switzerland; and Argami P, Department of Pathology, The Johns Hopkins University, Baltimore, USA); however, a typical expression of TFE3 and TFEB could not be demonstrated. Comparative genome hybridization (CGH) analysis did not reveal chromosomal imbalances such as losses at 3p or gains at 17q specific for clear cell RCC or papillary RCC, respectively (data not shown).
Besides the 5 cm tumor, multiple 1 to 2 mm nodules were observed in the adjacent renal tissue, which showed the 3 components of AMLs and the typical immunohistochemically expression of HMB-45 (Figure 1E and F).
Pathological findings of the lung tumors
Macroscopically, open-lung biopsies revealed 2 to 5 mm sharply demarcated and randomly distributed nodules in both lungs (Figure 2A).
The nodules were composed of proliferated and enlarged type II pneumocytes which had abundant eosinophilic cytoplasm and vesicular nuclei with prominent nucleoli and occasional eosinophilic inclusions. The cells formed ill-defined areas of papillae that filled the alveolar space and partly obscured the alveolar architecture. Significant atypia or mitosis could not be observed. The interalveolar septa were mild thickened with increased reticulin (Figure 2B, C, E, G). Immunohistochemically, the hyperplastic epithelial cells showed an expression of pan-CK, TTF-1 (Figure 2D, F), and EMA, whereas stains for HMB-45, actin, vimentin and ER were uniformly negative. The proliferation rate evaluated with MIB-1 was solely 2% (Figure 2H).
TSC is an autosomal-dominant disorder characterized by a variably high incidence (90-95%) affecting 0.5-1 per 10,000 births. The diagnosis of TSC is currently made by using the criteria established by Gomez . These criteria are composed of primary (e.g. subependymal nodes and facial angiofibroma), secondary, (e.g. AMLs and LAM), and tertiary features (e.g. hypomelanotic maculas). Whereas the hamartomas in TSC are benign lesions, other phakomatoses such as Von-Hippel-Lindau (VHL) disease are characterized by the development of malignant tumors. Therefore, RCC is a typical malignant tumor that is known to arise in VHL, whereas tuberous TSC patients also develop RCC, but only in rare cases . The mechanisms behind the occurrence of RCC could be demonstrated in the Eker rat model which develops RCCs based on a mutation in TSC2 gene [7–9]. Furthermore, an unusual pulmonary manifestation of TSC is MMPH, typically presenting multiple pulmonary nodules on chest roentgenogram or CT scan [4, 10, 11].
The case described here shows the diagnostic challenge of young TSC patients who present with multiple AMLs of the kidney and develop an unclassified RCC. RCC often occur in young TSC patients [12, 13] and demonstrate several subtypes . In our case, in the follow-up months a CT scan revealed multiple nodules in the lungs. It is difficult to differentiate between benign lesions like LAM or MMPH and metastasis on the basis of CT scans only, as our present case demonstrates . A definitive diagnosis of MMPH could only be made on the basis of histological examination of a lung biopsy. MMPH is extremely rare in TSC and in the literature less than 20 histologically documented cases are described and have been reported in association with LAM and AML . One of these cases shows MMPH in a TSC patient who had undergone a bilateral nephrectomy because of RCC. AML are not reported in this case, but the authors also describe the difficulty they had differentiating between the benign MMPH and metastasis of the RCC .
The association between TSC mutation and RCC seems to be often underestimated in familiarly RCC . Furthermore, the TSC 1/2 complex influences the beta-catenin pathway and could also play a functional role in other hereditary tumor syndromes such as Cowden’s disease or Peutz-Jeghers syndrome .
The case of a young TSC patient described here demonstrates a rare combination of AMLs, RCC and hamartomas in the lung, which posed a diagnostic dilemma.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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